A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439839



Internal ID21097392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36328531..36330667hg38UCSC Ensembl
chr9:36328528..36330664hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg382137
hg192137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439839
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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