A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121873



Internal ID18907121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:32938694..32939394hg38UCSC Ensembl
Outerchr14:33407900..33408600hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968531
SamplesKWS2
Known GenesNPAS3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121873
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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