A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370141



Internal ID21027694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13927401..13938360hg38UCSC Ensembl
chr3:13968898..13979860hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3810960
hg1910963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093936
Samples
Known GenesFGD5P1, TPRXL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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