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dbVar

Database of genomic structural variation

nsv6110571

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:2,187,710

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: 9115 SVs from 113 studies. See in: genome view

Submitted genomic47,903,487-50,091,196

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6110571	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	47,903,487	50,091,196
nsv6110571	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	48,406,744	50,594,453

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17627551	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17627551	Submitted genomic		NC_000019.10:g.479 03487_50091196inv	GRCh38 (hg38)		NC_000019.10	Chr19	47,903,487	50,091,196
nssv17627551	Remapped	Perfect	NC_000019.9:g.4840 6744_50594453inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	48,406,744	50,594,453

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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