A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177113



Internal ID20744153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133511608..133514768hg38UCSC Ensembl
chr9:136376730..136379890hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg383161
hg193161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450146
Supporting Variants
Samples
Known GenesTMEM8C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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