A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345856



Internal ID21003409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102719614..102720493hg38UCSC Ensembl
chr2:103336073..103336952hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205785
Samples
Known GenesMFSD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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