A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173920



Internal ID15879679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178690798..178707830hg38UCSC Ensembl
Innerchr1:178659933..178676965hg19UCSC Ensembl
Innerchr1:176926556..176943588hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3817033
hg1917033
hg1817033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548259
Supporting Variants
SamplesHGDP01415
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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