A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484367



Internal ID21141920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51063401..51064700hg38UCSC Ensembl
chr14:51530119..51531418hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019130
Samples
Known GenesTRIM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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