A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904801



Internal ID22679979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4276293..4316288hg38UCSC Ensembl
chr3:4317977..4357972hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3839996
hg1939996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424851
Samples
Known GenesSETMAR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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