A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447448



Internal ID21105001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73901606..73934670hg38UCSC Ensembl
chr10:75661364..75694428hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3833065
hg1933065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177434
Samples
Known GenesC10orf55, PLAU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447448
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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