A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251088



Internal ID20818128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45538419..45539001hg38UCSC Ensembl
chr1:46004091..46004673hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251088
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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