A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417493



Internal ID21075046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6517801..6813300hg38UCSC Ensembl
chr9:6517801..6813300hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38295500
hg19295500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7553n223
Supporting Variantsnssv18233342
Samples
Known GenesGLDC, KDM4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417493
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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