A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444248



Internal ID21101801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73962803..73987414hg38UCSC Ensembl
chr10:75722561..75747172hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3824612
hg1924612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444248
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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