A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552138



Internal ID20925268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72552929..72554336hg38UCSC Ensembl
chr3:72602080..72603487hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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