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dbVar

Database of genomic structural variation

nsv5966892

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: 83 SVs from 16 studies. See in: genome view

Submitted genomic169,993,907-169,993,907

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966892	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	169,993,907	169,993,907
nsv5966892	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	169,420,911	169,420,911

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17427272	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17427272	Submitted genomic		NC_000005.10:g.169 993907_169993908in s397	GRCh38 (hg38)		NC_000005.10	Chr5	169,993,907	169,993,907
nssv17427272	Remapped	Perfect	NC_000005.9:g.1694 20911_169420912ins 397	GRCh37.p13	First Pass	NC_000005.9	Chr5	169,420,911	169,420,911

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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