A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544454



Internal ID20917692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43326549..43326923hg38UCSC Ensembl
chr1:43792220..43792594hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544454
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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