A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069795



Internal ID19323190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51134645..51134986hg38UCSC Ensembl
chr14:51601363..51601704hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768387
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069795
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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