A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451269



Internal ID21108822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57669052..57677254hg38UCSC Ensembl
chr10:59428812..59437014hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg388203
hg198203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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