A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560193



Internal ID20933264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91251046..91660618hg38UCSC Ensembl
chr4:92172197..92581769hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38409573
hg19409573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265372
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560193
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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