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dbVar

Database of genomic structural variation

nsv5662232

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: 107 SVs from 24 studies. See in: genome view

Submitted genomic56,808,448-56,808,448

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5662232	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	56,808,448	56,808,448
nsv5662232	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	56,842,360	56,842,360

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17098530	insertion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17098530	Submitted genomic		NC_000016.10:g.568 08448_56808449ins7 4	GRCh38 (hg38)		NC_000016.10	Chr16	56,808,448	56,808,448
nssv17098530	Remapped	Perfect	NC_000016.9:g.5684 2360_56842361ins74	GRCh37.p13	First Pass	NC_000016.9	Chr16	56,842,360	56,842,360

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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