A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702500



Internal ID15439152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58622882..58628992hg38UCSC Ensembl
Innerchr20:57197938..57204048hg19UCSC Ensembl
Innerchr20:56631344..56637454hg18UCSC Ensembl
Innerchr20:56631344..56637454hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg386111
hg196111
hg186111
hg176111
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526233
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702500
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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