A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537169



Internal ID20910509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23912940..23914377hg38UCSC Ensembl
chr1:24239430..24240867hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381438
hg191438
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250078
Samples
Known GenesCNR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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