A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566835



Internal ID20939906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16757135..16757657hg38UCSC Ensembl
chr5:16757244..16757766hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267581
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566835
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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