A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635886



Internal ID18934167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18607196..18675639hg38UCSC Ensembl
Innerchr5:18607305..18675748hg19UCSC Ensembl
Innerchr5:18643062..18711505hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3868444
hg1968444
hg1868444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030684
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)nssv3635886
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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