A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528902



Internal ID15456195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76256651..76262034hg38UCSC Ensembl
Innerchr11:75967695..75973078hg19UCSC Ensembl
Innerchr11:75645343..75650726hg18UCSC Ensembl
Innerchr11:75645343..75650726hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg385384
hg195384
hg185384
hg175384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705586
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528902
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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