A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415768



Internal ID21073321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144902383..144992393hg38UCSC Ensembl
chr8:146127768..146217779hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3890011
hg1990012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222365
Samples
Known GenesZNF16, ZNF252P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415768
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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