A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547271



Internal ID20920473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151435521..151438069hg38UCSC Ensembl
chr1:151407997..151410545hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382549
hg192549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248150
Samples
Known GenesPOGZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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