A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524741



Internal ID15105348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40049473..40249892hg38UCSC Ensembl
Innerchr11:40071023..40271442hg19UCSC Ensembl
Innerchr11:40027599..40228018hg18UCSC Ensembl
Innerchr11:40027599..40228018hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38200420
hg19200420
hg18200420
hg17200420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv65n21
Supporting Variantsnssv700732
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524741
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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