A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059192



Internal ID19148411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61397486..61423823hg38UCSC Ensembl
Innerchr20:59972542..59998879hg19UCSC Ensembl
Innerchr20:59405937..59432274hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3826338
hg1926338
hg1826338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584448
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)nsv1059192
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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