A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251680



Internal ID20818720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2809549..3136794hg38UCSC Ensembl
chr20:2790195..3117440hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38327246
hg19327246
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599489
Supporting Variants
Samples
Known GenesAVP, C20orf141, GNRH2, MRPS26, OXT, PCED1A, PTPRA, TMEM239, UBOX5, UBOX5-AS1, VPS16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251680
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00022


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