A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434619



Internal ID21092172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73919049..73930636hg38UCSC Ensembl
chr8:74831284..74842871hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3811588
hg1911588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434619
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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