A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550796



Internal ID20923936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229491518..229492354hg38UCSC Ensembl
chr1:229627265..229628101hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250329
Samples
Known GenesNUP133
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550796
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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