A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431671



Internal ID22489541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31268745..31353868hg38UCSC Ensembl
chr6:31236522..31321645hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3885124
hg1985124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897473
Supporting Variants
Samples
Known GenesHLA-C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431671
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer