A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206442



Internal ID20773482
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 StatusS
Merged Variantsnsv6352619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206442
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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