A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055447



Internal ID18797978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34737641..35020344hg38UCSC Ensembl
Innerchr20:33325445..33608147hg19UCSC Ensembl
Innerchr20:32789106..33071808hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38282704
hg19282703
hg18282703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584744
Samples
Known GenesACSS2, GGT7, GSS, HMGB3P1, MIR499A, MIR499B, MYH7B, NCOA6, TRPC4AP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055447
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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