A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635922



Internal ID18934203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20712305..20967076hg38UCSC Ensembl
Innerchr5:20712414..20967185hg19UCSC Ensembl
Innerchr5:20748171..21002942hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38254772
hg19254772
hg18254772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019837
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)nssv3635922
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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