A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340894



Internal ID20998447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45159446..45915141hg38UCSC Ensembl
chr2:45386585..46142280hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38755696
hg19755696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3852n223
Supporting Variantsnssv18209806
Samples
Known GenesLINC01121, PRKCE, SRBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340894
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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