A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251041



Internal ID20818081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36054332..36054905hg38UCSC Ensembl
chr1:36519933..36520506hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541539
Supporting Variants
Samples
Known GenesAGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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