A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322608



Internal ID20855721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:194369697..194391275hg38UCSC Ensembl
chr1:194338827..194360405hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3821579
hg1921579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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