A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528846



Internal ID15109453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32252184..32310079hg38UCSC Ensembl
Innerchr18:29832147..29890042hg19UCSC Ensembl
Innerchr18:28086145..28144040hg18UCSC Ensembl
Innerchr18:28086145..28144040hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3857896
hg1957896
hg1857896
hg1757896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705525
Samples
Known GenesGAREM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528846
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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