A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356422



Internal ID21013975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64225096..64225680hg38UCSC Ensembl
chr3:64210772..64211356hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101487
Samples
Known GenesPRICKLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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