A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170561



Internal ID20737601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67899350..67910891hg38UCSC Ensembl
chr8:68811585..68823126hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3811542
hg1911542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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