A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370848



Internal ID21028401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13908400..14017716hg38UCSC Ensembl
chr3:13949897..14059216hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38109317
hg19109320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093923
Samples
Known GenesFGD5P1, TPRXL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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