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dbVar

Database of genomic structural variation

nsv6088488

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: 143 SVs from 27 studies. See in: genome view

Submitted genomic59,951,207-59,951,207

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6088488	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	59,951,207	59,951,207
nsv6088488	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	58,028,568	58,028,568

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17631410	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17631410	Submitted genomic		NC_000017.11:g.599 51207_59951208ins2 94	GRCh38 (hg38)		NC_000017.11	Chr17	59,951,207	59,951,207
nssv17631410	Remapped	Perfect	NC_000017.10:g.580 28568_58028569ins2 94	GRCh37.p13	First Pass	NC_000017.10	Chr17	58,028,568	58,028,568

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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