A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437260



Internal ID21094813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64450801..64561300hg38UCSC Ensembl
chr9:69463219..69573718hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38110500
hg19110500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7780n223
Supporting Variantsnssv18227799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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