A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036085



Internal ID18778616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62104387..62127010hg38UCSC Ensembl
Innerchr11:61871859..61894482hg19UCSC Ensembl
Innerchr11:61628435..61651058hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3822624
hg1922624
hg1822624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503328
Samples
Known GenesINCENP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036085
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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