A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166875



Internal ID20733915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41054413..41079090hg38UCSC Ensembl
chr8:40911932..40936609hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3824678
hg1924678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166875
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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