A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600466



Internal ID16387875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178917647..178925244hg38UCSC Ensembl
Innerchr5:178344648..178352245hg19UCSC Ensembl
Innerchr5:178277254..178284851hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387598
hg197598
hg187598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10203n54
Supporting Variantsnssv1046177
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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