A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578447



Internal ID21770490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81334358..81334459hg38UCSC Ensembl
chr8:82246593..82246694hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578447
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