A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153935



Internal ID15873475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52085511..52131895hg38UCSC Ensembl
Innerchr5:51381345..51427729hg19UCSC Ensembl
Innerchr5:51417102..51463486hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3846385
hg1946385
hg1846385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598162
Supporting Variants
SamplesHGDP00210
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153935
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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