A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3057001



Internal ID21188869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1980691..1980691hg38UCSC Ensembl
chr12:2089857..2089857hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14021680
SamplesNA12878
Known GenesDCP1B
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)nsv3057001
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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