A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333386



Internal ID20866562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12538835..12629033hg38UCSC Ensembl
chr1:12598865..12689039hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3890199
hg1990175
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199336
Samples
Known GenesDHRS3, MIR6730
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333386
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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