A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176308



Internal ID21315104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111414892..111414961hg38UCSC Ensembl
chr1:111957514..111957583hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949506
Supporting Variants
SamplesHG002
Known GenesOVGP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176308
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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