A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904422



Internal ID16198378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20224106..20225077hg38UCSC Ensembl
Innerchr2:20423867..20424838hg19UCSC Ensembl
Innerchr2:20287348..20288319hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38972
hg19972
hg18972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581161
Supporting Variants
Samples
Known GenesSDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904422
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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