A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv912170



Internal ID16206126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:71115461..71120352hg38UCSC Ensembl
Innerchr2:71342591..71347482hg19UCSC Ensembl
Innerchr2:71196099..71200990hg18UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg384892
hg194892
hg184892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582195
Supporting Variants
Samples
Known GenesMCEE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv912170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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