A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1046175



Internal ID15899361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178917647..178923708hg38UCSC Ensembl
Innerchr5:178344648..178350709hg19UCSC Ensembl
Innerchr5:178277254..178283315hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386062
hg196062
hg186062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600464
Supporting Variants
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1046175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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