A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635999



Internal ID18934280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29581537..29626117hg38UCSC Ensembl
Innerchr5:29581644..29626224hg19UCSC Ensembl
Innerchr5:29617401..29661981hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3844581
hg1944581
hg1844581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030155
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635999
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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