A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439729



Internal ID218261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173734535..173735670hg38UCSC Ensembl
chr3:173452325..173453460hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942830
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439729
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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