A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600469



Internal ID16387878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178921553..178923708hg38UCSC Ensembl
Innerchr5:178348554..178350709hg19UCSC Ensembl
Innerchr5:178281160..178283315hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382156
hg192156
hg182156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1046182, nssv1046187, nssv1046186, nssv1046191, nssv1046188, nssv1046184, nssv1046183, nssv1046181, nssv1046185, nssv1046189, nssv1046190
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600469
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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