A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001965



Internal ID21911308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68974118..68974244hg38UCSC Ensembl
chr8:69886353..69886479hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583405
Samples
Known GenesLOC100505718
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001965
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