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dbVar

Database of genomic structural variation

nsv435992

Organism: Homo sapiens

Study:nstd16 (Korbel et al. 2007)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:6,549

Publication(s):Korbel et al. 2007

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: 36 SVs from 2 studies. See in: genome view

Remapped(Score: Good):2,765-9,313

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv435992	Remapped	Good	GRCh38.p12	non-nuclear	First Pass	NC_012920.1	ChrMT	2,765	9,313
nsv435992	Remapped	Good	GRCh37.p13	non-nuclear	First Pass	NC_012920.1	ChrMT	2,765	9,313
nsv435992	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_001807.4	ChrMT	2,767	9,314

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv465783	inversion	SAMN00000376	Sequencing	Paired-end mapping	468

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv465783	Remapped	Good	NC_012920.1:g.(276 5_?)_(?_9313)inv	GRCh38.p12	First Pass	NC_012920.1	ChrMT	2,765	9,313
nssv465783	Remapped	Good	NC_012920.1:g.(276 5_?)_(?_9313)inv	GRCh37.p13	First Pass	NC_012920.1	ChrMT	2,765	9,313
nssv465783	Submitted genomic		NC_001807.4:g.(276 7_?)_(?_9314)inv	NCBI36 (hg18)		NC_001807.4	ChrMT	2,767	9,314

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

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