A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445578



Internal ID21103131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89058746..89059596hg38UCSC Ensembl
chr9:91673661..91674511hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189933
Samples
Known GenesSHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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