A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516446



Internal ID15443739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160248493..160293773hg38UCSC Ensembl
Innerchr5:159675500..159720780hg19UCSC Ensembl
Innerchr5:159608078..159653358hg18UCSC Ensembl
Innerchr5:159608078..159653358hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3845281
hg1945281
hg1845281
hg1745281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv359n21
Supporting Variantsnssv675097, nssv661847, nssv673607, nssv668459
Samples
Known GenesCCNJL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516446
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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