A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567508



Internal ID20940579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39601159..39601339hg38UCSC Ensembl
chr4:39602779..39602959hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265170
Samples
Known GenesSMIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567508
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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