A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508301



Internal ID284996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122022458..122023375hg38UCSC Ensembl
chr12:122460364..122461281hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17685059
Samples
Known GenesBCL7A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508301
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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