A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449827



Internal ID21107380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100259116..100279790hg38UCSC Ensembl
chr10:102018873..102039547hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3820675
hg1920675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185103
Samples
Known GenesBLOC1S2, CWF19L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449827
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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