A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162730



Internal ID20729770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104498780..104499076hg38UCSC Ensembl
chr8:105511008..105511304hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431118
Supporting Variants
Samples
Known GenesLRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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