A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171033



Internal ID20738073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87986544..87987227hg38UCSC Ensembl
chr8:88998772..88999455hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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