A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142220



Internal ID20709260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32659733..32755866hg38UCSC Ensembl
chr6:32627510..32723643hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3896134
hg1996134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409225
Supporting Variants
Samples
Known GenesHLA-DQA2, HLA-DQB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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