A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320294



Internal ID20853392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28534411..28556151hg38UCSC Ensembl
chr1:28860923..28882663hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3821741
hg1921741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203543
Samples
Known GenesRCC1, TRNAU1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320294
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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