A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528007



Internal ID15455300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69424843..69424973hg38UCSC Ensembl
Innerchr11:69239611..69239741hg19UCSC Ensembl
Innerchr11:68948792..68948922hg18UCSC Ensembl
Innerchr11:68948792..68948922hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38131
hg19131
hg18131
hg17131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704533
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528007
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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