A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171918



Internal ID20738958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81520818..81545088hg38UCSC Ensembl
chr8:82433053..82457323hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3824271
hg1924271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433055
Supporting Variants
Samples
Known GenesFABP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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