A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450169



Internal ID21107722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34922469..35053653hg38UCSC Ensembl
chr10:35211397..35342581hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38131185
hg19131185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv686n223
Supporting Variantsnssv18183803
Samples
Known GenesCUL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450169
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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