A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700527



Internal ID15437179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56440475..56445633hg38UCSC Ensembl
Innerchr20:55015531..55020689hg19UCSC Ensembl
Innerchr20:54448938..54454096hg18UCSC Ensembl
Innerchr20:54448938..54454096hg17UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg385159
hg195159
hg185159
hg175159
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524572
Supporting Variants
Samples
Known GenesCASS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700527
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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