A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171815



Internal ID20738855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94682772..94690884hg38UCSC Ensembl
chr8:95695000..95703112hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg388113
hg198113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431811
Supporting Variants
Samples
Known GenesESRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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