A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002845



Internal ID21912188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99429546..99629979hg38UCSC Ensembl
chr8:100441774..100642207hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38200434
hg19200434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595260
Samples
Known GenesMIR599, MIR875, VPS13B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002845
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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