A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319096



Internal ID20852188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106847669..106851507hg38UCSC Ensembl
chr1:107390291..107394129hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383839
hg193839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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