A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350809



Internal ID21008362
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 StatusM
Merged Variants
Supporting Variantsnssv18206574
Samples
Known GenesCLASP1, NIFK, NIFK-AS1, RNU4ATAC, TSN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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