A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257988



Internal ID21398215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17770798..17858431hg38UCSC Ensembl
chr12:17923732..18011365hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3887634
hg1987634
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730212
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257988
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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