A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319314



Internal ID20852408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226116435..226140212hg38UCSC Ensembl
chr1:226304136..226327913hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3823778
hg1923778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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