A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032003



Internal ID18774537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50585657hg38UCSC Ensembl
Innerchr5:49455624..49881491hg19UCSC Ensembl
Innerchr5:49491381..49917248hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38425868
hg19425868
hg18425868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642119
Samples
Known GenesEMB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032003
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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