A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249740



Internal ID20816780
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 StatusS
Merged Variantsnsv6540359
Supporting Variants
Samples
Known GenesFAM159A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249740
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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