A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084661



Internal ID21993894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57323418..57323418hg38UCSC Ensembl
chr10:59083178..59083178hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084661
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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