A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519980



Internal ID18471575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59032901..59092289hg38UCSC Ensembl
Innerchr11:58800374..58859762hg19UCSC Ensembl
Innerchr11:58556950..58616338hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3859389
hg1959389
hg1859389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050297
Supporting Variants
Samples
Known GenesLOC283194
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519980
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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