A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591977



Internal ID21784020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58211935..58211986hg38UCSC Ensembl
chr8:59124494..59124545hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005893
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591977
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