A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438787



Internal ID21096340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72556222..72570816hg38UCSC Ensembl
chr9:75171138..75185732hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3814595
hg1914595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220200
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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