A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568777



Internal ID20941848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39897264..39897512hg38UCSC Ensembl
chr4:39898884..39899132hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265205
Samples
Known GenesPDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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