A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165677



Internal ID20732717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132059551..132083565hg38UCSC Ensembl
chr8:133071798..133095812hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3824015
hg1924015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419989
Supporting Variants
Samples
Known GenesHHLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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