A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3640474



Internal ID18938755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99239249..99292611hg38UCSC Ensembl
Innerchr5:98574953..98628315hg19UCSC Ensembl
Innerchr5:98602853..98656215hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3853363
hg1953363
hg1853363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025867
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)nssv3640474
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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