A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169303



Internal ID20736343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64781461..64787688hg38UCSC Ensembl
chr8:65694018..65700245hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg386228
hg196228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431951
Supporting Variants
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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