A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062257



Internal ID19151476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78128482..78173537hg38UCSC Ensembl
Innerchr18:75888482..75933537hg19UCSC Ensembl
Innerchr18:73989470..74034525hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3845056
hg1945056
hg1845056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3408n100
Supporting Variantsnssv3723242
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)nsv1062257
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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