A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428611



Internal ID21086164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12956847..12986385hg38UCSC Ensembl
chr8:12814356..12843894hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3829539
hg1929539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217409
Samples
Known GenesKIAA1456
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428611
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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