A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516697



Internal ID15097304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:168486505..168486598hg38UCSC Ensembl
Innerchr5:167913510..167913603hg19UCSC Ensembl
Innerchr5:167846088..167846181hg18UCSC Ensembl
Innerchr5:167846088..167846181hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3894
hg1994
hg1894
hg1794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685425, nssv670211, nssv676877, nssv677952, nssv682891, nssv663011, nssv692457
Samples
Known GenesRARS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516697
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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