A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251000



Internal ID20818040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43474875..43475370hg38UCSC Ensembl
chr1:43940546..43941041hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251000
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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