A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3059585



Internal ID21191286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113263169..113263169hg38UCSC Ensembl
chr13:113917483..113917483hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14025977
SamplesCHM1
Known GenesCUL4A
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)nsv3059585
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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