A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600473



Internal ID16387882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178921553..178925819hg38UCSC Ensembl
Innerchr5:178348554..178352820hg19UCSC Ensembl
Innerchr5:178281160..178285426hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384267
hg194267
hg184267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10206n54
Supporting Variantsnssv1046202, nssv1046212, nssv1046210, nssv1046203, nssv1046206, nssv1046204, nssv1046215, nssv1046200, nssv1046214, nssv1046205, nssv1046211, nssv1046213, nssv1046201, nssv1046208, nssv1046207, nssv1046209
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600473
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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