A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066907



Internal ID18809438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47310827..47736827hg38UCSC Ensembl
Innerchr20:45939571..46365571hg19UCSC Ensembl
Innerchr20:45372978..45798978hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38426001
hg19426001
hg18426001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731360
Samples
Known GenesLOC100131496, NCOA3, SULF2, ZMYND8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066907
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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