A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331211



Internal ID20864373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95667301..95674000hg38UCSC Ensembl
chr1:96132857..96139556hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331211
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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