A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575264



Internal ID20948335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127234181..127235960hg38UCSC Ensembl
chr3:126953024..126954803hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575264
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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