A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171316



Internal ID20738356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76146257..76153918hg38UCSC Ensembl
chr8:77058492..77066153hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg387662
hg197662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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