A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437343



Internal ID21094896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69515001..69529400hg38UCSC Ensembl
chr10:71274757..71289156hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3814400
hg1914400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv801n223
Supporting Variantsnssv18189954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437343
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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