A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904426



Internal ID16198382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20224447..20225404hg38UCSC Ensembl
Innerchr2:20424208..20425165hg19UCSC Ensembl
Innerchr2:20287689..20288646hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38958
hg19958
hg18958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581164
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)nssv904426
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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