A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327865



Internal ID20861008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143527201..143738800hg38UCSC Ensembl
chr1:149021851..149233450hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38211600
hg19211600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv328n223
Supporting Variantsnssv18200150
Samples
Known GenesLOC101929780, NBPF23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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