A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327476



Internal ID20860615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:628601..649600hg38UCSC Ensembl
chr1:563981..584980hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3821000
hg1921000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203666
Samples
Known GenesMIR6723
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327476
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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