A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550156



Internal ID20923306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24748500..24749017hg38UCSC Ensembl
chr1:25074991..25075508hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251512
Samples
Known GenesCLIC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550156
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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