A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647006



Internal ID18945287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109491711..109523327hg38UCSC Ensembl
Innerchr5:108827412..108859028hg19UCSC Ensembl
Innerchr5:108855311..108886927hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3831617
hg1931617
hg1831617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030194
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)nssv3647006
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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