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dbVar

Database of genomic structural variation

nsv3934688

Organism: Homo sapiens

Study:nstd167 (Wenger et al. 2019)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):Wenger et al. 2019

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: 26 SVs from 6 studies. See in: genome view

Remapped(Score: Perfect):76,073,501-76,073,501

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3934688	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	76,073,501	76,073,501
nsv3934688	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	74,069,582	74,069,582

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv15185081	insertion	SAMN03283347	Sequencing	de novo and local sequence assembly	Heterozygous	30,634

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15185081	Remapped	Perfect	NC_000017.11:g.760 73501_76073502ins3 424	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,073,501	76,073,501
nssv15185081	Submitted genomic		NC_000017.10:g.740 69582_74069583ins3 424	GRCh37 (hg19)		NC_000017.10	Chr17	74,069,582	74,069,582

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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