A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527852



Internal ID15455145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26884318..26886529hg38UCSC Ensembl
Innerchr18:24464282..24466493hg19UCSC Ensembl
Innerchr18:22718280..22720491hg18UCSC Ensembl
Innerchr18:22718280..22720491hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382212
hg192212
hg182212
hg172212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704350
Samples
Known GenesAQP4-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527852
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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