A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165697



Internal ID20732737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132544216..132574422hg38UCSC Ensembl
chr8:133556463..133586670hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3830207
hg1930208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423215
Supporting Variants
Samples
Known GenesHPYR1, LRRC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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