A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906738



Internal ID22681941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122363277..122363873hg38UCSC Ensembl
chr3:122082124..122082720hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396301
Samples
Known GenesCCDC58
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906738
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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