A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249193



Internal ID20816233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100435739..100436499hg38UCSC Ensembl
chr1:100901295..100902055hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545634
Supporting Variants
Samples
Known GenesCDC14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249193
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00057


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