A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565287



Internal ID21889642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155399083..155399139hg38UCSC Ensembl
chr6:155720217..155720273hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003635
Supporting Variants
Samples
Known GenesNOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565287
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