A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058517



Internal ID19147736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61446730..61515326hg38UCSC Ensembl
Innerchr20:60021786..60090382hg19UCSC Ensembl
Innerchr20:59455181..59523777hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3868597
hg1968597
hg1868597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4342n100
Supporting Variantsnssv3584453
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)nsv1058517
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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