A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730379



Internal ID19028660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:921359..1034331hg38UCSC Ensembl
Innerchr20:902002..1014974hg19UCSC Ensembl
Innerchr20:850002..962974hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38112973
hg19112973
hg18112973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055853
Supporting Variants
Samples
Known GenesRSPO4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3730379
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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