A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527711



Internal ID15108318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54028627..54029002hg38UCSC Ensembl
Innerchr20:52645166..52645541hg19UCSC Ensembl
Innerchr20:52078573..52078948hg18UCSC Ensembl
Innerchr20:52078573..52078948hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38376
hg19376
hg18376
hg17376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704191
Samples
Known GenesBCAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527711
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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