A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436338



Internal ID214958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202955453..202955608hg38UCSC Ensembl
chr1:202924581..202924736hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16894722
Samples
Known GenesADIPOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436338
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