A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168860



Internal ID20735900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37087280..37087653hg38UCSC Ensembl
chr8:36944798..36945171hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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