A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029089



Internal ID19118308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:164866043..166021018hg38UCSC Ensembl
Innerchr5:164293049..165448023hg19UCSC Ensembl
Innerchr5:164225627..165380601hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381154976
hg191154975
hg181154975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648243
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)nsv1029089
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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