A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590941



Internal ID20964012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53860643..53862034hg38UCSC Ensembl
chr10:55620403..55621794hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218754
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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