A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766547



Internal ID18960950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111912775..111913376hg38UCSC Ensembl
chr11:111783499..111784100hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070987
Supporting Variants
SamplesKWP1
Known GenesHSPB2, HSPB2-C11orf52
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766547
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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