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dbVar

Database of genomic structural variation

nsv5955439

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: 179 SVs from 26 studies. See in: genome view

Submitted genomic174,087,503-174,087,503

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5955439	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	174,087,503	174,087,503
nsv5955439	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	174,952,231	174,952,231

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17395866	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17395866	Submitted genomic		NC_000002.12:g.174 087503_174087504in s735	GRCh38 (hg38)		NC_000002.12	Chr2	174,087,503	174,087,503
nssv17395866	Remapped	Perfect	NC_000002.11:g.174 952231_174952232in s735	GRCh37.p13	First Pass	NC_000002.11	Chr2	174,952,231	174,952,231

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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