A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540359



Internal ID20913650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52651237..52652670hg38UCSC Ensembl
chr1:53116909..53118342hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381434
hg191434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249740
Samples
Known GenesFAM159A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540359
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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