A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356550



Internal ID21014103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61814143..61844147hg38UCSC Ensembl
chr3:61799817..61829821hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3830005
hg1930005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101748
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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