A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250869



Internal ID20817909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32687379..32687856hg38UCSC Ensembl
chr1:33152980..33153457hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542685
Supporting Variants
Samples
Known GenesSYNC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250869
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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