A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434182



Internal ID21091735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3418576..3429191hg38UCSC Ensembl
chr9:3418576..3429191hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3810616
hg1910616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184388
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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