A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14022569



Internal ID21172736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146224809..146224864hg38UCSC Ensembl
chr3:145942596..145942651hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3050453
Supporting Variants
SamplesNA12878
Known GenesPLSCR4
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)nssv14022569
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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