A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318508



Internal ID20851600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86506956..86549222hg38UCSC Ensembl
chr1:86972639..87014905hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3842267
hg1942267
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205178
Samples
Known GenesCLCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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