A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423907



Internal ID21081460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86879218..87004561hg38UCSC Ensembl
chr8:87891446..88016789hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38125344
hg19125344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170892
Samples
Known GenesCNBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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