A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371677



Internal ID21029230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59786721..61760277hg38UCSC Ensembl
chr3:59772447..61745951hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381973557
hg191973505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212315
Samples
Known GenesFHIT, PTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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