A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257970



Internal ID21399036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17770044..17859281hg38UCSC Ensembl
chr12:17922978..18012215hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3889238
hg1989238
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730212
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257970
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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