A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419670



Internal ID21077223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101244759..101245586hg38UCSC Ensembl
chr8:102256987..102257814hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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