A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509868



Internal ID18808149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118486991..118497403hg38UCSC Ensembl
Innerchr11:118357706..118368118hg19UCSC Ensembl
Innerchr11:117862916..117873328hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3810413
hg1910413
hg1810413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043363
Supporting Variants
Samples
Known GenesKMT2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509868
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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