A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169619



Internal ID20736659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71336072..71346093hg38UCSC Ensembl
chr8:72248307..72258328hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3810022
hg1910022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428515
Supporting Variants
Samples
Known GenesEYA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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