A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661151



Internal ID15051117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45859560..45965589hg38UCSC Ensembl
Innerchr20:44488199..44594228hg19UCSC Ensembl
Innerchr20:43921606..44027635hg18UCSC Ensembl
Innerchr20:43921606..44027635hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38106030
hg19106030
hg18106030
hg17106030
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517296
Supporting Variants
Samples
Known GenesCTSA, NEURL2, PCIF1, PLTP, SPATA25, ZNF335, ZSWIM1, ZSWIM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661151
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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