A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050297



Internal ID18792828
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 StatusM
Merged Variantsdgv1208n100
Supporting Variantsnssv3519980
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)nsv1050297
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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