A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441682



Internal ID21099235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45258101..45262800hg38UCSC Ensembl
chr10:45753549..45758248hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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