A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113661



Internal ID19250953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:73488779..73488852hg38UCSC Ensembl
Outerchr14:73955484..73955557hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968977
SamplesKWS2
Known GenesHEATR4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113661
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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