Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

esv3809461

Organism: Homo sapiens

Study:estd192 (COSMIC)
Variant Type:complex chromosomal rearrangement
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:21

Description:Chr12:g.(111802400_111802420)_chr8:(95371246_9
5371266)bkpt
Publication(s):Forbes et al. 2008, Forbes et al. 2008

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 106 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):94,359,018-94,359,038

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
esv3809461	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	94,359,018	94,359,038	94,359,018	94,359,038
esv3809461	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	111,364,596	111,364,616	111,364,596	111,364,616
esv3809461	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	95,371,246	95,371,266	95,371,246	95,371,266
esv3809461	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	111,802,400	111,802,420	111,802,400	111,802,420

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv16638647	interchromosomal translocation	2196220	Curated	Curated	256

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop	strand
essv16638647	Remapped	Perfect	GRCh38.p12	First Pass	NC_000008.11	Chr8	94,359,018	94,359,038	94,359,018	94,359,038	not reported
essv16638647	Remapped	Perfect	GRCh38.p12	First Pass	NC_000012.12	Chr12	111,364,596	111,364,616	111,364,596	111,364,616	not reported
essv16638647	Submitted genomic		GRCh37 (hg19)		NC_000008.10	Chr8	95,371,246	95,371,266	95,371,246	95,371,266	not reported
essv16638647	Submitted genomic		GRCh37 (hg19)		NC_000012.11	Chr12	111,802,400	111,802,420	111,802,400	111,802,420	not reported

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

You are here: NCBI