A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056755



Internal ID19145974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60752864..60763029hg38UCSC Ensembl
Innerchr20:59327921..59338085hg19UCSC Ensembl
Innerchr20:58761316..58771480hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810166
hg1910165
hg1810165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584322
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056755
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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