A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435997



Internal ID214624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42912496..42912744hg38UCSC Ensembl
chr3:42953988..42954236hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931935
Samples
Known GenesZNF662
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435997
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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