A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153934



Internal ID15873973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52079355..52136835hg38UCSC Ensembl
Innerchr5:51375189..51432669hg19UCSC Ensembl
Innerchr5:51410946..51468426hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3857481
hg1957481
hg1857481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598161
Supporting Variants
SamplesHGDP00454
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153934
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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