A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661847



Internal ID15398499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160255770..160293773hg38UCSC Ensembl
Innerchr5:159682777..159720780hg19UCSC Ensembl
Innerchr5:159615355..159653358hg18UCSC Ensembl
Innerchr5:159615355..159653358hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3838004
hg1938004
hg1838004
hg1738004
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516446
Supporting Variants
Samples
Known GenesCCNJL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661847
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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