A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639421



Internal ID21587726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32587397..32587397hg38UCSC Ensembl
chr6:32555174..32555174hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156021
SamplesNA24385
Known GenesHLA-DRB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639421
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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