A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448713



Internal ID21106266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20742160..20755545hg38UCSC Ensembl
chr10:21031089..21044474hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3813386
hg1913386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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