A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352878



Internal ID21010431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118940919..118965897hg38UCSC Ensembl
chr2:119698495..119723473hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3824979
hg1924979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206545
Samples
Known GenesMARCO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352878
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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