A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232847



Internal ID20799888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26912161..26913023hg38UCSC Ensembl
chr12:27065094..27065956hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585829
Supporting Variants
Samples
Known GenesASUN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232847
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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