A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448370



Internal ID21105923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41480401..41487800hg38UCSC Ensembl
chr9:68169717..68177000hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg387400
hg197284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7742n223
Supporting Variantsnssv18227059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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