A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547261



Internal ID20920463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71198922..71199795hg38UCSC Ensembl
chr3:71248073..71248946hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4906n223
Supporting Variantsnssv18262885
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547261
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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