A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449039



Internal ID21106592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65706601..65739900hg38UCSC Ensembl
chr9:42687521..42720820hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3833300
hg1933300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7807n223
Supporting Variantsnssv18220733
Samples
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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