A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264247



Internal ID20831287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159121022..159122355hg38UCSC Ensembl
chr4:160042174..160043507hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264247
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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