A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063280



Internal ID18805811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21260355..21341420hg38UCSC Ensembl
Innerchr20:21240993..21322058hg19UCSC Ensembl
Innerchr20:21188993..21270058hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3881066
hg1981066
hg1881066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737173
Samples
Known GenesXRN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063280
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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