A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450343



Internal ID21107896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33013507..33049441hg38UCSC Ensembl
chr10:33302435..33338369hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3835935
hg1935935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450343
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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