A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164931



Internal ID20731971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126575283..126576866hg38UCSC Ensembl
chr8:127587528..127589111hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg381584
hg191584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429462
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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