A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558611



Internal ID20931682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150021278..150021537hg38UCSC Ensembl
chr3:149739065..149739324hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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