A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428722



Internal ID21086275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81521001..81526200hg38UCSC Ensembl
chr8:82433236..82438435hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7397n223
Supporting Variantsnssv18233741
Samples
Known GenesFABP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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