A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550435



Internal ID20923581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85900632..85900731hg38UCSC Ensembl
chr1:86366315..86366414hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251887
Samples
Known GenesCOL24A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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