A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023388



Internal ID83305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72525615..72562906hg38UCSC Ensembl
chr9:75140531..75177822hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3837292
hg1937292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489471
Supporting Variants
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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