A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024321



Internal ID19113538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133769093..133792957hg38UCSC Ensembl
Innerchr5:133104784..133128648hg19UCSC Ensembl
Innerchr5:133132683..133156547hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3823865
hg1923865
hg1823865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5809n100
Supporting Variantsnssv3648120
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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