A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164929



Internal ID20731969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126572752..126574406hg38UCSC Ensembl
chr8:127584997..127586651hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg381655
hg191655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00102


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