A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564685



Internal ID20937756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188600812..188602169hg38UCSC Ensembl
chr3:188318600..188319957hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381358
hg191358
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259915
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564685
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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