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dbVar

Database of genomic structural variation

nsv5653497

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: 168 SVs from 33 studies. See in: genome view

Submitted genomic64,861,515-64,861,515

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653497	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	64,861,515	64,861,515
nsv5653497	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	62,857,633	62,857,633

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17084824	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17084824	Submitted genomic		NC_000017.11:g.648 61515_64861516ins7 999	GRCh38 (hg38)		NC_000017.11	Chr17	64,861,515	64,861,515
nssv17084824	Remapped	Perfect	NC_000017.10:g.628 57633_62857634ins7 999	GRCh37.p13	First Pass	NC_000017.10	Chr17	62,857,633	62,857,633

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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