A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250886



Internal ID20817926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33681195..33681783hg38UCSC Ensembl
chr1:34146795..34147383hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552897
Supporting Variants
Samples
Known GenesCSMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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