A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569192



Internal ID20942263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39890818..39891926hg38UCSC Ensembl
chr4:39892438..39893546hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265202
Samples
Known GenesPDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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