A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322063



Internal ID20855172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54172045..54175655hg38UCSC Ensembl
chr1:54637718..54641328hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383611
hg193611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061536
Samples
Known GenesCYB5RL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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