A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554014



Internal ID20927123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37070177..37070574hg38UCSC Ensembl
chr3:37111668..37112065hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259986
Samples
Known GenesLRRFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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