A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438077



Internal ID216648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196918043..196918160hg38UCSC Ensembl
chr3:196644914..196645031hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944323
Samples
Known GenesSENP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438077
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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