A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543744



Internal ID20916990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22061237..22061595hg38UCSC Ensembl
chr1:22387730..22388088hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249278
Samples
Known GenesCDC42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543744
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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