A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539629



Internal ID20912925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114103333..114111746hg38UCSC Ensembl
chr1:114645955..114654368hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg388414
hg198414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249238
Samples
Known GenesSYT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539629
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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