A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579341



Internal ID20952412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13866735..13867290hg38UCSC Ensembl
chr10:13908735..13909290hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228577
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579341
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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