A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551903



Internal ID20925035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98019312..98019421hg38UCSC Ensembl
chr3:97738156..97738265hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262760
Samples
Known GenesGABRR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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