A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433766



Internal ID21091319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32951743..32969990hg38UCSC Ensembl
chr8:32809261..32827508hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3818248
hg1918248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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