A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326966



Internal ID20860103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39574201..39577800hg38UCSC Ensembl
chr1:40039873..40043472hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203078
Samples
Known GenesPABPC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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