A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437904



Internal ID21095457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24766106..24766501hg38UCSC Ensembl
chr10:25055035..25055430hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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