A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171831



Internal ID20738871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94830071..94831577hg38UCSC Ensembl
chr8:95842299..95843805hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381507
hg191507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431880
Supporting Variants
Samples
Known GenesINTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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