A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449810



Internal ID21107363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93680001..93682000hg38UCSC Ensembl
chr10:95439758..95441757hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985207
Samples
Known GenesFRA10AC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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