A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334096



Internal ID20867277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28336641..28366987hg38UCSC Ensembl
chr1:28663152..28693498hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3830347
hg1930347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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