A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568958



Internal ID20942029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25996714..25997627hg38UCSC Ensembl
chr4:25998336..25999249hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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