A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124737



Internal ID19253699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:33062879..33839733hg38UCSC Ensembl
Outerchr16:33074200..33642200hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38776855
hg19568001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976791
SamplesKWS2
Known GenesLOC390705, RNU6-76P, TP53TG3, TP53TG3B, TP53TG3C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124737
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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