A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331778



Internal ID20864945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85763009..85904334hg38UCSC Ensembl
chr1:86228692..86370017hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38141326
hg19141326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205171
Samples
Known GenesCOL24A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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