A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547621



Internal ID20920822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200581969..200582205hg38UCSC Ensembl
chr1:200551097..200551333hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248267
Samples
Known GenesKIF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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