A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437064



Internal ID215663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173073557..173074222hg38UCSC Ensembl
chr3:172791347..172792012hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941404
Samples
Known GenesSPATA16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437064
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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