A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442862



Internal ID21100415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63542401..63591600hg38UCSC Ensembl
chr9:68138135..68187334hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3849200
hg1949200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7767n223
Supporting Variantsnssv18218936
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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