A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170186



Internal ID20737226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75384075..75388961hg38UCSC Ensembl
chr8:76296310..76301196hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg384887
hg194887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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