A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536077



Internal ID20909430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193393051..193396827hg38UCSC Ensembl
chr1:193362181..193365957hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg383777
hg193777
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536077
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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