A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446133



Internal ID21103686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16451621..16474090hg38UCSC Ensembl
chr10:16493620..16516089hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822470
hg1922470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv621n223
Supporting Variantsnssv17978914
Samples
Known GenesPTER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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