A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028055



Internal ID16322011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25995995..26064694hg38UCSC Ensembl
Innerchr5:25996104..26064803hg19UCSC Ensembl
Innerchr5:26031861..26100560hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3868700
hg1968700
hg1868700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597636
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)nssv1028055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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