A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510144



Internal ID286772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73969797..74163166hg38UCSC Ensembl
chr12:74363577..74556946hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38193370
hg19193370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17689134
Samples
Known GenesLOC100507377
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510144
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer