A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026415



Internal ID16320371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18852292..18970362hg38UCSC Ensembl
Innerchr5:18852401..18970471hg19UCSC Ensembl
Innerchr5:18888158..19006228hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38118071
hg19118071
hg18118071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597381
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)nssv1026415
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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