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dbVar

Database of genomic structural variation

nsv5637677

Organism: Homo sapiens

Study:nstd207 (Ebert 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):Ebert 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: 90 SVs from 20 studies. See in: genome view

Submitted genomic140,427,461-140,427,461

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5637677	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	140,427,461	140,427,461
nsv5637677	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	139,807,046	139,807,046

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17138113	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17138113	Submitted genomic		NC_000005.10:g.140 427461_140427462in s226	GRCh38 (hg38)		NC_000005.10	Chr5	140,427,461	140,427,461
nssv17138113	Remapped	Perfect	NC_000005.9:g.1398 07046_139807047ins 226	GRCh37.p13	First Pass	NC_000005.9	Chr5	139,807,046	139,807,046

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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