A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527555



Internal ID15454848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107024306..107100755hg38UCSC Ensembl
Innerchr11:106895032..106971481hg19UCSC Ensembl
Innerchr11:106400242..106476691hg18UCSC Ensembl
Innerchr11:106400242..106476691hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3876450
hg1976450
hg1876450
hg1776450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704016
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527555
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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