A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543514



Internal ID20916760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93255244..93257226hg38UCSC Ensembl
chr1:93720801..93722783hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381983
hg191983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252752
Samples
Known GenesCCDC18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543514
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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