A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705888



Internal ID15095854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117820430..117821455hg38UCSC Ensembl
Innerchr11:117691145..117692170hg19UCSC Ensembl
Innerchr11:117196355..117197380hg18UCSC Ensembl
Innerchr11:117196355..117197380hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381026
hg191026
hg181026
hg171026
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517470
Supporting Variants
Samples
Known GenesFXYD2, FXYD6-FXYD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705888
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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