A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206574



Internal ID20773614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:121419207..121790649hg38UCSC Ensembl
chr2:122176783..122548225hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38371443
hg19371443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350809
Supporting Variants
Samples
Known GenesCLASP1, NIFK, NIFK-AS1, RNU4ATAC, TSN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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