A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028708



Internal ID15881894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28779250..28868356hg38UCSC Ensembl
Innerchr5:28779357..28868463hg19UCSC Ensembl
Innerchr5:28815114..28904220hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3889107
hg1989107
hg1889107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597715
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)nssv1028708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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