A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435971



Internal ID21093524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12176955..12177530hg38UCSC Ensembl
chr10:12218954..12219529hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195569
Samples
Known GenesNUDT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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