A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564508



Internal ID20937579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2129588..2130117hg38UCSC Ensembl
chr4:2131315..2131844hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265557
Samples
Known GenesPOLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564508
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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