A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536283



Internal ID20909636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100280831..100281723hg38UCSC Ensembl
chr1:100746387..100747279hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249189
Samples
Known GenesMIR553, RTCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536283
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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