A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205564



Internal ID20772604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155303311..155324993hg38UCSC Ensembl
chr2:156159823..156181505hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3821683
hg1921683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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