A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573960



Internal ID21766003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46166212..46166277hg38UCSC Ensembl
chr6:46133949..46134014hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013291
Supporting Variants
Samples
Known GenesENPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573960
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