A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541348



Internal ID20914630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74952533..74958985hg38UCSC Ensembl
chr1:75418217..75424669hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg386453
hg196453
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541348
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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