A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443925



Internal ID21101478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36659027..36684523hg38UCSC Ensembl
chr10:36947955..36973451hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3825497
hg1925497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443925
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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