A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434804



Internal ID213471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68784941..68784997hg38UCSC Ensembl
chr3:68834092..68834148hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934027
Samples
Known GenesFAM19A4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434804
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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