A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445376



Internal ID21102929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95004301..95006200hg38UCSC Ensembl
chr9:97766583..97768482hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182696
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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