A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163479



Internal ID20730519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115200966..115205283hg38UCSC Ensembl
chr8:116213195..116217512hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384318
hg194318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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