A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859035



Internal ID22633970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72684077..72685176hg38UCSC Ensembl
chr9:75298993..75300092hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514252, nssv17514251
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859035
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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