A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179938



Internal ID20746978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72549780..72553066hg38UCSC Ensembl
chr9:75164696..75167982hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383287
hg193287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445951
Supporting Variants
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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