A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436281



Internal ID21093834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94873231..94880876hg38UCSC Ensembl
chr9:97635513..97643158hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387646
hg197646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186288
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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