A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560954



Internal ID20934025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26460551..26461185hg38UCSC Ensembl
chr4:26462173..26462807hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560954
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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