A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645904



Internal ID18944185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102577045..102669334hg38UCSC Ensembl
Innerchr5:101912749..102005038hg19UCSC Ensembl
Innerchr5:101940648..102032937hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3892290
hg1992290
hg1892290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033405
Supporting Variants
Samples
Known GenesLINC00491, LINC00492
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3645904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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