A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029078



Internal ID19118297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:34156377..34234025hg38UCSC Ensembl
Innerchr5:34156482..34234130hg19UCSC Ensembl
Innerchr5:34192239..34269887hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3877649
hg1977649
hg1877649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745962
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)nsv1029078
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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