A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067387



Internal ID19156606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61439901..61511162hg38UCSC Ensembl
Innerchr20:60014957..60086218hg19UCSC Ensembl
Innerchr20:59448352..59519613hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3871262
hg1971262
hg1871262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4342n100
Supporting Variantsnssv3584451
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)nsv1067387
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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