A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450749



Internal ID21108302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97983101..97986900hg38UCSC Ensembl
chr9:100745383..100749182hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191910
Samples
Known GenesANP32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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