A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206491



Internal ID20773531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113064901..113421800hg38UCSC Ensembl
chr2:113822478..114179377hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38356900
hg19356900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337104
Supporting Variants
Samples
Known GenesIL1F10, IL1RN, PAX8, PAX8-AS1, PSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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