A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565012



Internal ID20938083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157517636..157517946hg38UCSC Ensembl
chr4:158438788..158439098hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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