A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449357



Internal ID21106910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62921501..62932400hg38UCSC Ensembl
chr10:64681261..64692160hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv763n223
Supporting Variantsnssv18192044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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