A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174146



Internal ID20741186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116638898..116862678hg38UCSC Ensembl
chr9:119401177..119624957hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38223781
hg19223781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440976
Supporting Variants
Samples
Known GenesASTN2, TRIM32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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