A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561113



Internal ID20934184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157205113..157205213hg38UCSC Ensembl
chr4:158126265..158126365hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561113
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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