A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435326



Internal ID213977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194894073..195018172hg38UCSC Ensembl
chr3:194614802..194738901hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38124100
hg19124100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435326
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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