A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438004



Internal ID21095557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68793262..68796382hg38UCSC Ensembl
chr10:70553019..70556139hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383121
hg193121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438004
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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