A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438581



Internal ID21096134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80219901..80260600hg38UCSC Ensembl
chr10:81979657..82020356hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3840700
hg1940700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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