A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435707



Internal ID21093260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34881089..35029485hg38UCSC Ensembl
chr10:35170017..35318413hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38148397
hg19148397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv686n223
Supporting Variantsnssv18180604
Samples
Known GenesCUL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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