A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352619



Internal ID21010172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85067308..85069217hg38UCSC Ensembl
chr2:85294431..85296340hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381910
hg191910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352619
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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