A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546011



Internal ID20919231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39346244..39346642hg38UCSC Ensembl
chr1:39811916..39812314hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253067
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546011
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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