A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087770



Internal ID21997003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20718199..20718199hg38UCSC Ensembl
chr10:21007128..21007128hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087770
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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