A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451572



Internal ID21109125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64433401..64551600hg38UCSC Ensembl
chr9:69445819..69564018hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38118200
hg19118200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7780n223
Supporting Variantsnssv18232953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451572
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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