A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422845



Internal ID21080398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144360727..144401977hg38UCSC Ensembl
chr8:145584387..145627371hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3841251
hg1942985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228128
Samples
Known GenesADCK5, CPSF1, MIR1234, MIR6849, MIR939, SLC52A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422845
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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