A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526844



Internal ID15107451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131645762..131649041hg38UCSC Ensembl
Innerchr11:131515656..131518935hg19UCSC Ensembl
Innerchr11:131020866..131024145hg18UCSC Ensembl
Innerchr11:131020866..131024145hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383280
hg193280
hg183280
hg173280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703202
Samples
Known GenesNTM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526844
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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