A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539728



Internal ID20913023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:191793913..191794233hg38UCSC Ensembl
chr1:191763043..191763363hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539728
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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