A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448411



Internal ID21105964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45186467..45189971hg38UCSC Ensembl
chr10:45681915..45685419hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383505
hg193505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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