A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551418



Internal ID20924552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232406698..232412559hg38UCSC Ensembl
chr1:232542444..232548305hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg385862
hg195862
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250638
Samples
Known GenesSIPA1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551418
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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