A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519751



Internal ID15447044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42102899..42225168hg38UCSC Ensembl
Innerchr11:42124449..42246718hg19UCSC Ensembl
Innerchr11:42081025..42203294hg18UCSC Ensembl
Innerchr11:42081025..42203294hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38122270
hg19122270
hg18122270
hg17122270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697031
Samples
Known GenesLOC100507205
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519751
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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