A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635949



Internal ID18934230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24560072..24578029hg38UCSC Ensembl
Innerchr5:24560181..24578138hg19UCSC Ensembl
Innerchr5:24595938..24613895hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3817958
hg1917958
hg1817958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022665
Supporting Variants
Samples
Known GenesCDH10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635949
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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