A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642146



Internal ID18593741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:56490012..56541040hg38UCSC Ensembl
Innerchr5:55785839..55836867hg19UCSC Ensembl
Innerchr5:55821596..55872624hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3851029
hg1951029
hg1851029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026100
Supporting Variants
Samples
Known GenesLOC101928448
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642146
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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