A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035636



Internal ID19124855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29732363..29829581hg38UCSC Ensembl
Innerchr11:29753910..29851128hg19UCSC Ensembl
Innerchr11:29710486..29807704hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3897219
hg1997219
hg1897219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503983
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035636
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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