A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445025



Internal ID21102578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133518523..133518925hg38UCSC Ensembl
chr9:136383645..136384047hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177115
Samples
Known GenesTMEM8C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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