A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069922



Internal ID19318556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158991309..158996409hg38UCSC Ensembl
chr1:158961099..158966199hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770246
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069922
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