A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448715



Internal ID21106268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56352901..56357400hg38UCSC Ensembl
chr10:58112662..58117161hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448715
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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