A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425802



Internal ID21083355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1600745..2098778hg38UCSC Ensembl
chr9:1600745..2098778hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38498034
hg19498034
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235693
Samples
Known GenesSMARCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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