A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256573



Internal ID21398658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17769997..17859246hg38UCSC Ensembl
chr12:17922931..18012180hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3889250
hg1989250
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730212
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256573
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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