A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578485



Internal ID21526954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125607064..125609145hg38UCSC Ensembl
chr6:125928210..125930291hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157624
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578485
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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