A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430818



Internal ID21088371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82808882..83072901hg38UCSC Ensembl
chr8:83721117..83985136hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38264020
hg19264020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7401n223
Supporting Variantsnssv18221309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430818
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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