A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538142



Internal ID20911466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71460420..71461636hg38UCSC Ensembl
chr3:71509571..71510787hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262895
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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