A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541133



Internal ID20914418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221959647..221972418hg38UCSC Ensembl
chr1:222132989..222145760hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3812772
hg1912772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541133
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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