A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528829



Internal ID15456122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85784226..85785249hg38UCSC Ensembl
Innerchr11:85495269..85496292hg19UCSC Ensembl
Innerchr11:85172917..85173940hg18UCSC Ensembl
Innerchr11:85172917..85173940hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381024
hg191024
hg181024
hg171024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705503
Samples
Known GenesSYTL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528829
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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