A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029191



Internal ID19118410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176932135..176958816hg38UCSC Ensembl
Innerchr5:176359136..176385817hg19UCSC Ensembl
Innerchr5:176291742..176318423hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3826682
hg1926682
hg1826682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649285
Samples
Known GenesUIMC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029191
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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