A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153308



Internal ID15880285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28806149..28902719hg38UCSC Ensembl
Innerchr5:28806256..28902826hg19UCSC Ensembl
Innerchr5:28842013..28938583hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3896571
hg1996571
hg1896571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597729
Supporting Variants
SamplesNINDS_189
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153308
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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