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dbVar

Database of genomic structural variation

nsv6081475

Organism: Homo sapiens

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

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

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: 104 SVs from 17 studies. See in: genome view

Submitted genomic110,295,559-110,295,559

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6081475	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	110,295,559	110,295,559
nsv6081475	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	112,055,317	112,055,317

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17581252	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17581252	Submitted genomic		NC_000010.11:g.110 295559_110295560in s245	GRCh38 (hg38)		NC_000010.11	Chr10	110,295,559	110,295,559
nssv17581252	Remapped	Perfect	NC_000010.10:g.112 055317_112055318in s245	GRCh37.p13	First Pass	NC_000010.10	Chr10	112,055,317	112,055,317

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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