A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373896



Internal ID21031449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69212344..69222727hg38UCSC Ensembl
chr3:69261495..69271878hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3810384
hg1910384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104376
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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