A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441915



Internal ID220363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37208749..37208892hg38UCSC Ensembl
chr2:37435892..37436035hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911467
Samples
Known GenesCEBPZ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441915
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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