A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586662



Internal ID20959733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15059239..15059843hg38UCSC Ensembl
chr10:15101238..15101842hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219018
Samples
Known GenesOLAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586662
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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