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dbVar

Database of genomic structural variation

nsv4754141

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: 275 SVs from 19 studies. See in: genome view

Remapped(Score: Perfect):59,152,239-59,152,239

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4754141	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	59,152,239	59,152,239
nsv4754141	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	56,819,471	56,819,471

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16280506	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16280506	Remapped	Perfect	NC_000018.10:g.591 52239_59152240ins3 01	GRCh38.p12	First Pass	NC_000018.10	Chr18	59,152,239	59,152,239
nssv16280506	Submitted genomic		NC_000018.9:g.5681 9471_56819472ins30 1	GRCh37 (hg19)		NC_000018.9	Chr18	56,819,471	56,819,471

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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