A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1039449



Internal ID15892635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99009478..99021711hg38UCSC Ensembl
Innerchr5:98345182..98357415hg19UCSC Ensembl
Innerchr5:98373082..98385315hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3812234
hg1912234
hg1812234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599100
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1039449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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