A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522782



Internal ID15450075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22847391..22869557hg38UCSC Ensembl
Innerchr11:22868937..22891103hg19UCSC Ensembl
Innerchr11:22825513..22847679hg18UCSC Ensembl
Innerchr11:22825513..22847679hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3822167
hg1922167
hg1822167
hg1722167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698425
Samples
Known GenesCCDC179
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522782
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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