A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088323



Internal ID21997556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59908702..59908702hg38UCSC Ensembl
chr10:61668460..61668460hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088323
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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