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dbVar

Database of genomic structural variation

nsv5978736

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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: 224 SVs from 25 studies. See in: genome view

Submitted genomic45,238,875-45,238,875

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5978736	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	45,238,875	45,238,875
nsv5978736	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	45,634,756	45,634,756

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17394859	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17394859	Submitted genomic		NC_000022.11:g.452 38875_45238876ins7 8	GRCh38 (hg38)		NC_000022.11	Chr22	45,238,875	45,238,875
nssv17394859	Remapped	Perfect	NC_000022.10:g.456 34756_45634757ins7 8	GRCh37.p13	First Pass	NC_000022.10	Chr22	45,634,756	45,634,756

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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