A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251239



Internal ID20818279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6551661..6552382hg38UCSC Ensembl
chr1:6611721..6612442hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552717
Supporting Variants
Samples
Known GenesNOL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251239
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00034


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