A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771276



Internal ID19314346
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 StatusS
Merged Variantsnsv1070630
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771276
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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