A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050928



Internal ID19140147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126801755..126858448hg38UCSC Ensembl
Innerchr11:126671650..126728343hg19UCSC Ensembl
Innerchr11:126176860..126233553hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3856694
hg1956694
hg1856694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517467
Samples
Known GenesKIRREL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050928
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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