A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168856



Internal ID20735896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37026746..37040892hg38UCSC Ensembl
chr8:36884264..36898410hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3814147
hg1914147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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