A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205618



Internal ID20772658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21647797..21711660hg38UCSC Ensembl
chr2:21870669..21934532hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3863864
hg1963864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355037
Supporting Variants
Samples
Known GenesLOC645949
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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