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

dbVar

Database of genomic structural variation

nsv5621276

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

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: 334 SVs from 43 studies. See in: genome view

Submitted genomic6,448,901-6,448,901

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5621276	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	6,448,901	6,448,901
nsv5621276	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	6,508,961	6,508,961

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17066213	insertion	SAMN00249812	Sequencing	Sequence alignment	1,255

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17066213	Submitted genomic		NC_000001.11:g.644 8901_6448902ins145	GRCh38 (hg38)		NC_000001.11	Chr1	6,448,901	6,448,901
nssv17066213	Remapped	Perfect	NC_000001.10:g.650 8961_6508962ins145	GRCh37.p13	First Pass	NC_000001.10	Chr1	6,508,961	6,508,961

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI