A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172864



Internal ID20739904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9241170..9370248hg38UCSC Ensembl
chr8:9098680..9227758hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38129079
hg19129079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418545
Supporting Variants
Samples
Known GenesLOC157273
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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