A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1038114



Internal ID15891300
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 StatusS
Merged Variantsnsv598965
Supporting Variants
Samples
Known GenesLOC102546227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1038114
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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