A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441039



Internal ID21098592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65728701..65748200hg38UCSC Ensembl
chr9:42709621..42729120hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3819500
hg1919500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234517
Samples
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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