A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1045482



Internal ID15551982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172657047..172700301hg38UCSC Ensembl
Innerchr5:172084050..172127304hg19UCSC Ensembl
Innerchr5:172016655..172059909hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3843255
hg1943255
hg1843255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600289
Supporting Variants
Samples
Known GenesNEURL1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1045482
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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