A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3055489



Internal ID21187427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100345001..100345001hg38UCSC Ensembl
chr14:100811338..100811338hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14032674
SamplesNA12878
Known GenesWARS
MethodSequencing
AnalysisCombines the NGS (e.g., Illumina) and SMS (e.g., Pacbio) for detecting large and small SVs (parameters the same as commit eee31f6 of https://bitbucket.org/xianfan/hybridassemblysv)
Platform
Comments
ReferenceFan_et_al_2017
Pubmed ID28104618
Accession Number(s)nsv3055489
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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