A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569234



Internal ID20942305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147714281..147715348hg38UCSC Ensembl
chr4:148635432..148636499hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569234
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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