A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429965



Internal ID208794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9062839..9062988hg38UCSC Ensembl
chr1:9122898..9123047hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890074
Samples
Known GenesSLC2A5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429965
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