A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257085



Internal ID21399563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17770892..17860319hg38UCSC Ensembl
chr12:17923826..18013253hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3889428
hg1989428
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730212
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257085
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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