A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035143



Internal ID15541643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:76790772..76833228hg38UCSC Ensembl
Innerchr5:76086597..76129053hg19UCSC Ensembl
Innerchr5:76122353..76164809hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3842457
hg1942457
hg1842457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598683
Supporting Variants
Samples
Known GenesF2RL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035143
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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