A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056528



Internal ID19145747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60990189..61016904hg38UCSC Ensembl
Innerchr20:59565245..59591960hg19UCSC Ensembl
Innerchr20:58998640..59025355hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3826716
hg1926716
hg1826716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4340n100
Supporting Variantsnssv3731506
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)nsv1056528
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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