A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251037



Internal ID20818077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36045456..36047025hg38UCSC Ensembl
chr1:36511057..36512626hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539396
Supporting Variants
Samples
Known GenesAGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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