A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153029



Internal ID15855226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902228..9928750hg38UCSC Ensembl
Innerchr5:9902340..9928862hg19UCSC Ensembl
Innerchr5:9955340..9981862hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3826523
hg1926523
hg1826523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597095
Supporting Variants
Samples1780862516_A
Known GenesLOC285692
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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