A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553562



Internal ID15994285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16090634..16198743hg38UCSC Ensembl
Innerchr11:16112180..16220289hg19UCSC Ensembl
Innerchr11:16068756..16176865hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38108110
hg19108110
hg18108110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768277
Samples
Known GenesSOX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer