A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445902



Internal ID21103455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15493467..15495159hg38UCSC Ensembl
chr10:15535466..15537158hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381693
hg191693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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