A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902824



Internal ID22677985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115925466..115931137hg38UCSC Ensembl
chr3:115644313..115649984hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg385672
hg195672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397428
Samples
Known GenesLSAMP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902824
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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