A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437825



Internal ID21095378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64017001..64071300hg38UCSC Ensembl
chrUn_gl000211:48554..102853hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3854300
hg1954300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7774n223
Supporting Variantsnssv18236249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437825
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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