A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523327



Internal ID15103934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44064137..44071747hg38UCSC Ensembl
Innerchr11:44085687..44093297hg19UCSC Ensembl
Innerchr11:44042263..44049873hg18UCSC Ensembl
Innerchr11:44042263..44049873hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387611
hg197611
hg187611
hg177611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699071
Samples
Known GenesACCS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523327
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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