A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429504



Internal ID21087057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12966017..12977676hg38UCSC Ensembl
chr8:12823526..12835185hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3811660
hg1911660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165040
Samples
Known GenesKIAA1456
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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