A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670662



Internal ID15407314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:73150938..73155894hg38UCSC Ensembl
Innerchr5:72446765..72451721hg19UCSC Ensembl
Innerchr5:72482521..72487477hg18UCSC Ensembl
Innerchr5:72482521..72487477hg17UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg384957
hg194957
hg184957
hg174957
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517209
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670662
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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