A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988509



Internal ID15935779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2056748..2059880hg38UCSC Ensembl
Innerchr4:2058475..2061607hg19UCSC Ensembl
Innerchr4:2028273..2031405hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383133
hg193133
hg183133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593365
Supporting Variants
Samples
Known GenesNAT8L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988509
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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