A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030573



Internal ID19119792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84491086..84616693hg38UCSC Ensembl
Innerchr5:83786904..83912511hg19UCSC Ensembl
Innerchr5:83822660..83948267hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38125608
hg19125608
hg18125608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5710n100
Supporting Variantsnssv3639156, nssv3639157, nssv3639158
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)nsv1030573
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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