A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169806



Internal ID20736846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63241881..63243451hg38UCSC Ensembl
chr8:64154439..64156009hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415979
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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