A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561057



Internal ID20934128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55994327..55995032hg38UCSC Ensembl
chr4:56860493..56861198hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266436
Samples
Known GenesCEP135
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561057
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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