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dbVar

Database of genomic structural variation

nsv5971729

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 23 studies. See in: genome view

Submitted genomic24,045,417-24,045,417

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5971729	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	24,045,417	24,045,417
nsv5971729	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	21,625,381	21,625,381

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17372693	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17372693	Submitted genomic		NC_000018.10:g.240 45417_24045418ins3 15	GRCh38 (hg38)		NC_000018.10	Chr18	24,045,417	24,045,417
nssv17372693	Remapped	Perfect	NC_000018.9:g.2162 5381_21625382ins31 5	GRCh37.p13	First Pass	NC_000018.9	Chr18	21,625,381	21,625,381

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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