A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647098



Internal ID18945379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116197368..116269758hg38UCSC Ensembl
Innerchr5:115533065..115605455hg19UCSC Ensembl
Innerchr5:115560964..115633354hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3872391
hg1972391
hg1872391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016585
Supporting Variants
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3647098
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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