A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443946



Internal ID21101499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94855606..94857586hg38UCSC Ensembl
chr9:97617888..97619868hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190638
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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