A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171739



Internal ID20738779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93328685..93329064hg38UCSC Ensembl
chr8:94340913..94341292hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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