A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562455



Internal ID20935526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:130771234..133265562hg38UCSC Ensembl
chr4:131692389..134186717hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg382494329
hg192494329
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263046
Samples
Known GenesPCDH10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562455
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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