A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536139



Internal ID20909493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116455120..116468992hg38UCSC Ensembl
chr1:116997742..117011614hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3813873
hg1913873
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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