A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435791



Internal ID21093344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71704046..72013838hg38UCSC Ensembl
chr10:73463803..73773596hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38309793
hg19309794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187135
Samples
Known GenesC10orf105, C10orf54, CDH23, CHST3, MIR7152, PSAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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