A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586286



Internal ID20959357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119134391..119134888hg38UCSC Ensembl
chr10:120893903..120894400hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223515
Samples
Known GenesFAM45A, FAM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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