A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171845



Internal ID20738885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95195366..95204221hg38UCSC Ensembl
chr8:96207594..96216449hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg388856
hg198856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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