A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675097



Internal ID15411749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160259496..160264295hg38UCSC Ensembl
Innerchr5:159686503..159691302hg19UCSC Ensembl
Innerchr5:159619081..159623880hg18UCSC Ensembl
Innerchr5:159619081..159623880hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384800
hg194800
hg184800
hg174800
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)nssv675097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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