A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570266



Internal ID20943337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123249510..123250409hg38UCSC Ensembl
chr3:122968357..122969256hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262443
Samples
Known GenesSEC22A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570266
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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