A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424795



Internal ID21082348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2506703..2589019hg38UCSC Ensembl
chr9:2506703..2589019hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3882317
hg1982317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225732
Samples
Known GenesFLJ35024
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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