A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064324



Internal ID19153543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74415709..74472982hg38UCSC Ensembl
Innerchr18:72082944..72140217hg19UCSC Ensembl
Innerchr18:70233924..70291197hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3857274
hg1957274
hg1857274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563024
Samples
Known GenesFAM69C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064324
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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