A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516602



Internal ID15443895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50871424..50871978hg38UCSC Ensembl
Innerchr13:51445560..51446114hg19UCSC Ensembl
Innerchr13:50343561..50344115hg18UCSC Ensembl
Innerchr13:50343561..50344115hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38555
hg19555
hg18555
hg17555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691013, nssv678185, nssv689017, nssv686443, nssv690440, nssv681501, nssv669498, nssv660620, nssv671289, nssv657578, nssv671223, nssv679192, nssv661320
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516602
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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