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dbVar

Database of genomic structural variation

nsv7044886

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:3,059,437

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: 13077 SVs from 122 studies. See in: genome view

Submitted genomic185,127,051-188,186,487

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7044886	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	185,127,051	188,186,487
nsv7044886	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	186,048,205	189,107,641

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18774013	inversion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18774013	Submitted genomic		NC_000004.12:g.185 127051_188186487in v	GRCh38 (hg38)		NC_000004.12	Chr4	185,127,051	188,186,487
nssv18774013	Remapped	Perfect	NC_000004.11:g.186 048205_189107641in v	GRCh37.p13	First Pass	NC_000004.11	Chr4	186,048,205	189,107,641

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)
nssv18774013	2.1e-05	5	273374

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