A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575584



Internal ID21767627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37793324..37793386hg38UCSC Ensembl
chr8:37650842..37650904hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575584
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