A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153991



Internal ID15853212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121600538..121696680hg38UCSC Ensembl
Innerchr5:120936233..121032375hg19UCSC Ensembl
Innerchr5:120964132..121060274hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3896143
hg1996143
hg1896143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599622
Supporting Variants
Samples1780846321_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153991
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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