A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439760



Internal ID21097313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95528744..95536348hg38UCSC Ensembl
chr9:98291026..98298630hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387605
hg197605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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