A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442043



Internal ID22499913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31268646..31353767hg38UCSC Ensembl
chr6:31236423..31321544hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3885122
hg1985122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900955
Supporting Variants
Samples
Known GenesHLA-C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442043
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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