A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010364



Internal ID21919707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55203391..55210107hg38UCSC Ensembl
chr8:56115951..56122667hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg386717
hg196717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583737
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010364
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