A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007529



Internal ID21916872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35625993..35626073hg38UCSC Ensembl
chr6:35593770..35593850hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574145
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007529
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