A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642327



Internal ID21590632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32663118..32663118hg38UCSC Ensembl
chr6:32630895..32630895hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143908
SamplesHG00731
Known GenesHLA-DQB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642327
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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