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dbVar

Database of genomic structural variation

nsv4768279

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

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

Publication(s):Quan et al. 2021

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: 126 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):30,928,609-30,928,609

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4768279	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	30,928,609	30,928,609
nsv4768279	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	30,950,156	30,950,156

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16276113	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16276113	Remapped	Perfect	NC_000011.10:g.309 28609_30928610ins1 558	GRCh38.p12	First Pass	NC_000011.10	Chr11	30,928,609	30,928,609
nssv16276113	Submitted genomic		NC_000011.9:g.3095 0156_30950157ins15 58	GRCh37 (hg19)		NC_000011.9	Chr11	30,950,156	30,950,156

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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