A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251036



Internal ID20818076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36041059..36041260hg38UCSC Ensembl
chr1:36506660..36506861hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543117
Supporting Variants
Samples
Known GenesAGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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