A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432532



Internal ID21090085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54331862..54344497hg38UCSC Ensembl
chr8:55244422..55257057hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3812636
hg1912636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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