A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444765



Internal ID21102318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73249827..73271261hg38UCSC Ensembl
chr10:75009585..75031019hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3821435
hg1921435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195513
Samples
Known GenesDNAJC9-AS1, MRPS16, TTC18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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