A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444051



Internal ID21101604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133559901..133566400hg38UCSC Ensembl
chr10:135373405..135379904hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183942
Samples
Known GenesSYCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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