A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554264



Internal ID20927367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39194549..39197951hg38UCSC Ensembl
chr1:39660221..39663623hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383403
hg193403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253062
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554264
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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