A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416152



Internal ID21073705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33908578..33910416hg38UCSC Ensembl
chr8:33766096..33767934hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381839
hg191839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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