A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173771



Internal ID15876572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15192296..15224029hg38UCSC Ensembl
Innerchr1:15518792..15550525hg19UCSC Ensembl
Innerchr1:15391379..15423112hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3831734
hg1931734
hg1831734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545593
Supporting Variants
SamplesHGDP00863
Known GenesTMEM51
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173771
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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