A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561153



Internal ID21885508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32587399..32587399hg38UCSC Ensembl
chr6:32555176..32555176hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063480
Supporting Variants
Samples
Known GenesHLA-DRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561153
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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