A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766087



Internal ID18963466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17452700..17454501hg38UCSC Ensembl
chr10:17494699..17496500hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068286
Supporting Variants
SamplesKWP1
Known GenesST8SIA6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766087
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