A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562913



Internal ID20935984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169802702..169803661hg38UCSC Ensembl
chr3:169520490..169521449hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260462
Samples
Known GenesLRRC34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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