A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026301



Internal ID16320257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17347597..17353205hg38UCSC Ensembl
Innerchr5:17347706..17353314hg19UCSC Ensembl
Innerchr5:17400706..17406314hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385609
hg195609
hg185609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597315
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)nssv1026301
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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