A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546955



Internal ID20920166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109417954..109418440hg38UCSC Ensembl
chr1:109960576..109961062hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247300
Samples
Known GenesPSMA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546955
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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