A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430258



Internal ID21087811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6692102..6910990hg38UCSC Ensembl
chr9:6692102..6910990hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38218889
hg19218889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7558n223
Supporting Variantsnssv18228833
Samples
Known GenesKDM4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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