A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954203



Internal ID21374273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179901187..179901239hg38UCSC Ensembl
chr3:179618975..179619027hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180653
SamplesHG002
Known GenesPEX5L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954203
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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