A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367755



Internal ID21025308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61132070..61357923hg38UCSC Ensembl
chr3:61117743..61343597hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38225854
hg19225855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212332
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367755
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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