A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451609



Internal ID21109162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136216265..136255246hg38UCSC Ensembl
chr9:139108111..139147092hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3838982
hg1938982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7959n223
Supporting Variantsnssv18219226
Samples
Known GenesQSOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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