A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205771



Internal ID20772811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101495957..101500338hg38UCSC Ensembl
chr2:102112419..102116800hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg384382
hg194382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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