A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009624



Internal ID21918967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91816530..91816627hg38UCSC Ensembl
chr8:92828758..92828855hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009624
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