A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1096486



Internal ID15949672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143125117..143200731hg38UCSC Ensembl
Innerchr7:142822210..142897824hg19UCSC Ensembl
Innerchr7:142532332..142607946hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3875615
hg1975615
hg1875615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608659
Supporting Variants
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1096486
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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