A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251208



Internal ID20818248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50653491..50653790hg38UCSC Ensembl
chr1:51119163..51119462hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554338
Supporting Variants
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251208
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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