A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528205



Internal ID15108812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40049473..40246547hg38UCSC Ensembl
Innerchr11:40071023..40268097hg19UCSC Ensembl
Innerchr11:40027599..40224673hg18UCSC Ensembl
Innerchr11:40027599..40224673hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38197075
hg19197075
hg18197075
hg17197075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv65n21
Supporting Variantsnssv704766
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528205
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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