A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433522



Internal ID21091075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39956328..39959380hg38UCSC Ensembl
chr8:39813847..39816899hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg383053
hg193053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218755
Samples
Known GenesIDO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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