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dbVar

Database of genomic structural variation

nsv6112638

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: 109 SVs from 18 studies. See in: genome view

Submitted genomic16,410,181-16,410,181

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112638	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	16,410,181	16,410,181
nsv6112638	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	16,390,826	16,390,826

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17624667	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17624667	Submitted genomic		NC_000020.11:g.164 10181_16410182ins7 1	GRCh38 (hg38)		NC_000020.11	Chr20	16,410,181	16,410,181
nssv17624667	Remapped	Perfect	NC_000020.10:g.163 90826_16390827ins7 1	GRCh37.p13	First Pass	NC_000020.10	Chr20	16,390,826	16,390,826

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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