A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170375



Internal ID20737415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73525842..73526204hg38UCSC Ensembl
chr8:74438077..74438439hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428936
Supporting Variants
Samples
Known GenesSTAU2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00077


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