A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579992



Internal ID21528477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89128474..89128523hg38UCSC Ensembl
chr6:89838193..89838242hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148889
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579992
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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