A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536064



Internal ID20909417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117274222..117274716hg38UCSC Ensembl
chr1:117816844..117817338hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536064
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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