A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420587



Internal ID21078140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63883342..63892272hg38UCSC Ensembl
chr8:64795899..64804829hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg388931
hg198931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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