A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447347



Internal ID21104900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95084456..95130122hg38UCSC Ensembl
chr9:97846738..97892404hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3845667
hg1945667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178651
Samples
Known GenesC9orf3, FANCC, MIR23B, MIR24-1, MIR27B, MIR3074
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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