A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525706



Internal ID15452999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6965195..6991683hg38UCSC Ensembl
Innerchr11:6986426..7012914hg19UCSC Ensembl
Innerchr11:6943002..6969490hg18UCSC Ensembl
Innerchr11:6943002..6969490hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826489
hg1926489
hg1826489
hg1726489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701867
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525706
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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