A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439083



Internal ID217629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15531932..15532515hg38UCSC Ensembl
chr3:15573439..15574022hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439083
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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