A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016735



Internal ID19105952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:21784691..21813745hg38UCSC Ensembl
Innerchr5:21784800..21813854hg19UCSC Ensembl
Innerchr5:21820557..21849611hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3829055
hg1929055
hg1829055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635939
Samples
Known GenesCDH12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016735
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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