A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002657



Internal ID21912000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117924330..117924388hg38UCSC Ensembl
chr6:118245493..118245551hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563625
Samples
Known GenesSLC35F1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002657
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