A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453997



Internal ID21111550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97616221..97616711hg38UCSC Ensembl
chr9:100378503..100378993hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180327
Samples
Known GenesTSTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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