A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541913



Internal ID20915181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42971581..42972818hg38UCSC Ensembl
chr1:43437252..43438489hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250990
Samples
Known GenesSLC2A1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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