A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155229



Internal ID15534623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129757804..129805111hg38UCSC Ensembl
Innerchr7:129397644..129444951hg19UCSC Ensembl
Innerchr7:129184880..129232187hg18UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3847308
hg1947308
hg1847308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608420
Supporting Variants
SamplesNINDS_98
Known GenesMIR182, MIR183, MIR96
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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