A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14019366



Internal ID21170610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6565995..6565995hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3044794
Supporting Variants
SamplesNA12878
Known Genes
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)nssv14019366
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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