A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027978



Internal ID19117196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84477630..84616693hg38UCSC Ensembl
Innerchr5:83773448..83912511hg19UCSC Ensembl
Innerchr5:83809204..83948267hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38139064
hg19139064
hg18139064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5710n100
Supporting Variantsnssv3639152, nssv3639151
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)nsv1027978
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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