A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164652



Internal ID20731692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125008193..125013456hg38UCSC Ensembl
chr8:126020435..126025698hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385264
hg195264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435315
Supporting Variants
Samples
Known GenesSQLE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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