A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321429



Internal ID20854534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84145913..84155041hg38UCSC Ensembl
chr1:84611596..84620724hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg389129
hg199129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064407
Samples
Known GenesPRKACB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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