A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325121



Internal ID20858251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86544094..86624224hg38UCSC Ensembl
chr1:87009777..87089907hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3880131
hg1980131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205181
Samples
Known GenesCLCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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