A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3054767



Internal ID21186730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120082905..120083601hg38UCSC Ensembl
chr11:119953614..119954310hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14024101
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)nsv3054767
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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