A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577880



Internal ID20950951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124813209..124814363hg38UCSC Ensembl
chr10:126501778..126502932hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235947
Samples
Known GenesFAM175B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577880
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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