A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523512



Internal ID15450805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58622882..58637092hg38UCSC Ensembl
Innerchr20:57197938..57212148hg19UCSC Ensembl
Innerchr20:56631344..56645554hg18UCSC Ensembl
Innerchr20:56631344..56645554hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3814211
hg1914211
hg1814211
hg1714211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699284
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523512
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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