A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451490



Internal ID21109043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21275637..21280639hg38UCSC Ensembl
chr10:21564566..21569568hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg385003
hg195003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451490
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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