A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526587



Internal ID15107194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31049873..31059582hg38UCSC Ensembl
Innerchr18:28629839..28639548hg19UCSC Ensembl
Innerchr18:26883837..26893546hg18UCSC Ensembl
Innerchr18:26883837..26893546hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg389710
hg199710
hg189710
hg179710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702905
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526587
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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