A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642590



Internal ID21590895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68733737..68733737hg38UCSC Ensembl
chr6:69443629..69443629hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148871
SamplesHG03371
Known GenesBAI3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642590
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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