A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165061



Internal ID20732101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129970902..129982525hg38UCSC Ensembl
chr8:130983148..130994771hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3811624
hg1911624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415987
Supporting Variants
Samples
Known GenesFAM49B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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