A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207813



Internal ID20774853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89839977..90399163hg38UCSC Ensembl
chr2:89878787..90321525hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38559187
hg19442739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207813
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00363


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