A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415894



Internal ID21073447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60276601..60283500hg38UCSC Ensembl
chr8:61189160..61196059hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227340
Samples
Known GenesCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415894
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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