A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176913



Internal ID20743953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128794390..128795452hg38UCSC Ensembl
chr9:131556669..131557731hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436156
Supporting Variants
Samples
Known GenesTBC1D13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01922


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