A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324324



Internal ID20857449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209737834..209765280hg38UCSC Ensembl
chr1:209911179..209938625hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3827447
hg1927447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199917
Samples
Known GenesTRAF3IP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324324
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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