A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511617



Internal ID288193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116480758..116486200hg38UCSC Ensembl
chr10:118240270..118245712hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385443
hg195443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040685
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511617
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