A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056464



Internal ID19145683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76695215..76759346hg38UCSC Ensembl
Innerchr18:74407171..74471302hg19UCSC Ensembl
Innerchr18:72536159..72600290hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3864132
hg1964132
hg1864132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n100
Supporting Variantsnssv3563033
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)nsv1056464
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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