A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528149



Internal ID15455442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6278786..6280383hg38UCSC Ensembl
Innerchr11:6300016..6301613hg19UCSC Ensembl
Innerchr11:6256592..6258189hg18UCSC Ensembl
Innerchr11:6256592..6258189hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381598
hg191598
hg181598
hg171598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704696
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528149
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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