A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454983



Internal ID21112536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33162124..33193648hg38UCSC Ensembl
chr10:33451052..33482576hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3831525
hg1931525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181725
Samples
Known GenesNRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454983
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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