A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3049242



Internal ID21181290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12370313..12370836hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14018496
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)nsv3049242
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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