A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053752



Internal ID19142971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111413921..111440592hg38UCSC Ensembl
Innerchr11:111284646..111311317hg19UCSC Ensembl
Innerchr11:110789856..110816527hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3826672
hg1926672
hg1826672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520200
Samples
Known GenesLOC100132078
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053752
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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