A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334598



Internal ID20867785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235889490..235909879hg38UCSC Ensembl
chr1:236052790..236073179hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3820390
hg1920390
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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