A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586438



Internal ID16373847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61693013..61721678hg38UCSC Ensembl
Innerchr20:60268069..60296734hg19UCSC Ensembl
Innerchr20:59701464..59730129hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3828666
hg1928666
hg1828666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7641n54
Supporting Variantsnssv1151401
SamplesHGDP00161
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586438
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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