A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701382



Internal ID15091348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63221277..63323323hg38UCSC Ensembl
Innerchr20:61852629..61954675hg19UCSC Ensembl
Innerchr20:61323074..61425120hg18UCSC Ensembl
Innerchr20:61323074..61425120hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38102047
hg19102047
hg18102047
hg17102047
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525279
Supporting Variants
Samples
Known GenesARFGAP1, BIRC7, COL20A1, FLJ16779, MIR3196, MIR4326, NKAIN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701382
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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