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dbVar

Database of genomic structural variation

nsv5961786

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: 186 SVs from 50 studies. See in: genome view

Submitted genomic15,026,487-15,026,487

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961786	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	15,026,487	15,026,487
nsv5961786	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	15,166,611	15,166,611

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17393955	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17393955	Submitted genomic		NC_000002.12:g.150 26487_15026488ins1 76	GRCh38 (hg38)		NC_000002.12	Chr2	15,026,487	15,026,487
nssv17393955	Remapped	Perfect	NC_000002.11:g.151 66611_15166612ins1 76	GRCh37.p13	First Pass	NC_000002.11	Chr2	15,166,611	15,166,611

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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