A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036555



Internal ID19125774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134899517..135021453hg38UCSC Ensembl
Innerchr11:134769411..134891347hg19UCSC Ensembl
Innerchr11:134274621..134396557hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38121937
hg19121937
hg18121937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710796
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)nsv1036555
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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