A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327991



Internal ID20861135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209771296..209771667hg38UCSC Ensembl
chr1:209944641..209945012hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199919
Samples
Known GenesTRAF3IP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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