A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561670



Internal ID20934741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187482166..187483328hg38UCSC Ensembl
chr3:187199954..187201116hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381163
hg191163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561670
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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