A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527671



Internal ID15454964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74415709..74476151hg38UCSC Ensembl
Innerchr18:72082944..72143386hg19UCSC Ensembl
Innerchr18:70233924..70294366hg18UCSC Ensembl
Innerchr18:70233924..70294366hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3860443
hg1960443
hg1860443
hg1760443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704146
Samples
Known GenesFAM69C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527671
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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