A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440832



Internal ID21098385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65709201..65725200hg38UCSC Ensembl
chr9:42690121..42706120hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3816000
hg1916000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7809n223
Supporting Variantsnssv18230385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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