A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439993



Internal ID21097546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34789420..35085292hg38UCSC Ensembl
chr10:35078348..35374220hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38295873
hg19295873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv683n223
Supporting Variantsnssv18187996
Samples
Known GenesCUL2, PARD3, PARD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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