A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070630



Internal ID19317554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24696903..24697105hg38UCSC Ensembl
chr14:25166109..25166311hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771276
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070630
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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