A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169501



Internal ID20736541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69478487..69480302hg38UCSC Ensembl
chr8:70390722..70392537hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg381816
hg191816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432962
Supporting Variants
Samples
Known GenesSULF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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