A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553355



Internal ID20926463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92954665..92955750hg38UCSC Ensembl
chr1:93420222..93421307hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv270n223
Supporting Variantsnssv18252728
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553355
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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