A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328880



Internal ID20862030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165900164..165911997hg38UCSC Ensembl
chr1:165869401..165881234hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3811834
hg1911834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052849
Samples
Known GenesMIR3658, UCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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