A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565024



Internal ID20938095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145648436..145648938hg38UCSC Ensembl
chr4:146569588..146570090hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264788
Samples
Known GenesMMAA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565024
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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