A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424234



Internal ID21081787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64172046..64230360hg38UCSC Ensembl
chr8:65084603..65142917hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3858315
hg1958315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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