A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349541



Internal ID21007094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:117898895..117926046hg38UCSC Ensembl
chr2:118656471..118683622hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3827152
hg1927152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206541
Samples
Known GenesCCDC93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349541
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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