A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206099



Internal ID20773139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225226601..225233200hg38UCSC Ensembl
chr2:226091318..226097917hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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