A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257208



Internal ID21399010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14782578..14821065hg38UCSC Ensembl
chr16:14876435..14914922hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3838488
hg1938488
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730140
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257208
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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