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dbVar

Database of genomic structural variation

nsv6112637

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:133,901

Publication(s):Wu 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: 574 SVs from 65 studies. See in: genome view

Submitted genomic193,877,798-194,011,698

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112637	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	193,877,798	194,011,698
nsv6112637	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	194,742,522	194,876,422

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17520574	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17520574	Submitted genomic		NC_000002.12:g.193 877798_194011698in v	GRCh38 (hg38)		NC_000002.12	Chr2	193,877,798	194,011,698
nssv17520574	Remapped	Perfect	NC_000002.11:g.194 742522_194876422in v	GRCh37.p13	First Pass	NC_000002.11	Chr2	194,742,522	194,876,422

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.

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