A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438696



Internal ID21096249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22311201..22320400hg38UCSC Ensembl
chr10:22600130..22609329hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197082
Samples
Known GenesCOMMD3, COMMD3-BMI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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