A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450207



Internal ID21107760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96410089..96411834hg38UCSC Ensembl
chr9:99172371..99174116hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381746
hg191746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187951
Samples
Known GenesZNF367
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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