A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251179



Internal ID20818219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49114557..49118576hg38UCSC Ensembl
chr1:49580229..49584248hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg384020
hg194020
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543776
Supporting Variants
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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