A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069036



Internal ID18970057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28533170..28534071hg38UCSC Ensembl
chr10:28822099..28823000hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763434
SamplesKWP1
Known GenesWAC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069036
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