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dbVar

Database of genomic structural variation

nsv6561154

Organism: Homo sapiens

Study:nstd223 (Sedlazeck et al. 2020)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,011

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: 101 SVs from 23 studies. See in: genome view

Submitted genomic101,587,203-101,589,213

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6561154	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	101,587,203	101,589,213
nsv6561154	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	104,349,485	104,351,495

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18279331	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18279331	Submitted genomic		NC_000009.12:g.101 587203_101589213in v	GRCh38 (hg38)		NC_000009.12	Chr9	101,587,203	101,589,213
nssv18279331	Remapped	Perfect	NC_000009.11:g.104 349485_104351495in v	GRCh37.p13	First Pass	NC_000009.11	Chr9	104,349,485	104,351,495

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18279331	<0.001	1	39304

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