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dbVar

Database of genomic structural variation

nsv5647676

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: 140 SVs from 29 studies. See in: genome view

Submitted genomic64,783,558-64,783,558

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5647676	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	64,783,558	64,783,558
nsv5647676	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	62,779,676	62,779,676

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17092425	insertion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17092425	Submitted genomic		NC_000017.11:g.647 83558_64783559ins8 34	GRCh38 (hg38)		NC_000017.11	Chr17	64,783,558	64,783,558
nssv17092425	Remapped	Perfect	NC_000017.10:g.627 79676_62779677ins8 34	GRCh37.p13	First Pass	NC_000017.10	Chr17	62,779,676	62,779,676

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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