A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575982



Internal ID21768025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125702298..125707309hg38UCSC Ensembl
chr6:126023444..126028455hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385012
hg195012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007624
Supporting Variants
Samples
Known GenesLOC643623
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575982
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