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dbVar

Database of genomic structural variation

nsv6102553

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:2,995,519

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: 13011 SVs from 128 studies. See in: genome view

Submitted genomic18,724,785-21,720,303

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6102553	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	18,724,785	21,720,303
nsv6102553	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	18,835,595	21,903,105

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17634421	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17634421	Submitted genomic		NC_000019.10:g.187 24785_21720303inv	GRCh38 (hg38)		NC_000019.10	Chr19	18,724,785	21,720,303
nssv17634421	Remapped	Good	NC_000019.9:g.1883 5595_21903105inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	18,835,595	21,903,105

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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