A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527910



Internal ID15455203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9743801..9747516hg38UCSC Ensembl
Innerchr11:9765348..9769063hg19UCSC Ensembl
Innerchr11:9721924..9725639hg18UCSC Ensembl
Innerchr11:9721924..9725639hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383716
hg193716
hg183716
hg173716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704416
Samples
Known GenesSWAP70
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527910
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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