A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417469



Internal ID21075022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25819396..25830109hg38UCSC Ensembl
chr8:25676912..25687625hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3810714
hg1910714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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