A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435162



Internal ID213814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180613332..180614010hg38UCSC Ensembl
chr3:180331120..180331798hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944652
Samples
Known GenesCCDC39
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435162
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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