A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1045485



Internal ID15551985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172768130..172771179hg38UCSC Ensembl
Innerchr5:172195133..172198182hg19UCSC Ensembl
Innerchr5:172127738..172130788hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg383050
hg193050
hg183051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600294
Supporting Variants
Samples
Known GenesDUSP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1045485
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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