A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449868



Internal ID21107421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34197950..34392077hg38UCSC Ensembl
chr9:34197948..34392075hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38194128
hg19194128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7693n223
Supporting Variantsnssv18221644
Samples
Known GenesC9orf24, KIAA1161, KIF24, NUDT2, UBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449868
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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