A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447900



Internal ID226190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81656772..81657536hg38UCSC Ensembl
chr3:81705923..81706687hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936264
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447900
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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