A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598965



Internal ID16386374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97599035..97766112hg38UCSC Ensembl
Innerchr5:96934739..97101816hg19UCSC Ensembl
Innerchr5:96960495..97127572hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38167078
hg19167078
hg18167078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9937n54
Supporting Variantsnssv1038114
Samples
Known GenesLOC102546227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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