A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069990



Internal ID19318840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28400593..28402994hg38UCSC Ensembl
chr14:28869799..28872200hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772961
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069990
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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