A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026100



Internal ID18768632
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 StatusM
Merged Variants
Supporting Variantsnssv3642146
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)nsv1026100
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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