A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525136



Internal ID15452429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125075650..125076338hg38UCSC Ensembl
Innerchr11:124945546..124946234hg19UCSC Ensembl
Innerchr11:124450756..124451444hg18UCSC Ensembl
Innerchr11:124450756..124451444hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38689
hg19689
hg18689
hg17689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701206
Samples
Known GenesSLC37A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525136
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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