A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249522



Internal ID20816562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1842065..1948209hg38UCSC Ensembl
chr1:1773504..1879648hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38106145
hg19106145
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535955
Supporting Variants
Samples
Known GenesCALML6, GNB1, TMEM52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249522
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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