A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324086



Internal ID20857210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108181501..108234400hg38UCSC Ensembl
chr1:108724123..108777022hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3852900
hg1952900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199214
Samples
Known GenesNBPF4, SLC25A24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324086
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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