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dbVar

Database of genomic structural variation

nsv6062739

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: 81 SVs from 21 studies. See in: genome view

Submitted genomic55,169,205-55,169,205

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6062739	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	55,169,205	55,169,205
nsv6062739	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	54,465,033	54,465,033

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17548124	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17548124	Submitted genomic		NC_000005.10:g.551 69205_55169206ins3 19	GRCh38 (hg38)		NC_000005.10	Chr5	55,169,205	55,169,205
nssv17548124	Remapped	Perfect	NC_000005.9:g.5446 5033_54465034ins31 9	GRCh37.p13	First Pass	NC_000005.9	Chr5	54,465,033	54,465,033

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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