A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703065



Internal ID15439717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128797907..128798197hg38UCSC Ensembl
Innerchr11:128667802..128668092hg19UCSC Ensembl
Innerchr11:128173012..128173302hg18UCSC Ensembl
Innerchr11:128173012..128173302hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38291
hg19291
hg18291
hg17291
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526725
Supporting Variants
Samples
Known GenesFLI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703065
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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