A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449164



Internal ID21106717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93769501..93771300hg38UCSC Ensembl
chr9:96531783..96533582hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449164
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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