A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433695



Internal ID21091248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105004385..105012425hg38UCSC Ensembl
chr8:106016613..106024653hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg388041
hg198041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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