A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069822



Internal ID19316721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102591362..102591963hg38UCSC Ensembl
chr14:103057699..103058300hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770321
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069822
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