A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134581



Internal ID18902249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89117034..89117085hg38UCSC Ensembl
Outerchr16:89183442..89183493hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972461
SamplesKWS2
Known GenesACSF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134581
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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