A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576787



Internal ID20949858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52226903..52227369hg38UCSC Ensembl
chr15:52519100..52519566hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240373
Samples
Known GenesMYO5C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576787
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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