A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581536



Internal ID20954607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13853561..13854449hg38UCSC Ensembl
chr10:13895561..13896449hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232454
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581536
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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