A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153008



Internal ID15856002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8703036..8757929hg38UCSC Ensembl
Innerchr5:8703148..8758041hg19UCSC Ensembl
Innerchr5:8756148..8811041hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3854894
hg1954894
hg1854894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597051
Supporting Variants
Samples1798860306_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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