A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369164



Internal ID21026717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58572598..58573319hg38UCSC Ensembl
chr3:58558325..58559046hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102948
Samples
Known GenesFAM107A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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