A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209166



Internal ID20776206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:29839157..30061106hg38UCSC Ensembl
chr2:30062023..30283972hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38221950
hg19221950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353790
Supporting Variants
Samples
Known GenesALK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209166
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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