A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547919



Internal ID20921118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93274124..93275408hg38UCSC Ensembl
chr1:93739681..93740965hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381285
hg191285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv271n223
Supporting Variantsnssv18252753
Samples
Known GenesCCDC18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547919
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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