A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554556



Internal ID20927649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69235508..69236340hg38UCSC Ensembl
chr3:69284659..69285491hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4904n223
Supporting Variantsnssv18262858
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554556
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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