A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447295



Internal ID225604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25989980..25997637hg38UCSC Ensembl
chr2:26212849..26220506hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg387658
hg197658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447295
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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