A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060501



Internal ID19149720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61446730..61510594hg38UCSC Ensembl
Innerchr20:60021786..60085650hg19UCSC Ensembl
Innerchr20:59455181..59519045hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3863865
hg1963865
hg1863865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4342n100
Supporting Variantsnssv3731549, nssv3584452
Samples
Known GenesCDH4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060501
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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