A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355730



Internal ID21013283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59715696..61038029hg38UCSC Ensembl
chr3:59701422..61023701hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381322334
hg191322280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212313
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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