A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555383



Internal ID20928473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110363364..110364791hg38UCSC Ensembl
chr1:110905986..110907413hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247375
Samples
Known GenesSLC16A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555383
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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