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dbVar

Database of genomic structural variation

nsv5633944

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: 198 SVs from 37 studies. See in: genome view

Submitted genomic44,961,744-44,961,744

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5633944	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	44,961,744	44,961,744
nsv5633944	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	45,001,343	45,001,343

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17145463	insertion	SAMN00000419	Sequencing	Sequence alignment	1,071

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17145463	Submitted genomic		NC_000007.14:g.449 61744_44961745ins1 29	GRCh38 (hg38)		NC_000007.14	Chr7	44,961,744	44,961,744
nssv17145463	Remapped	Perfect	NC_000007.13:g.450 01343_45001344ins1 29	GRCh37.p13	First Pass	NC_000007.13	Chr7	45,001,343	45,001,343

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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