A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437529



Internal ID21095082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118434159..118501800hg38UCSC Ensembl
chr9:121196437..121264078hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3867642
hg1967642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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