A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256351



Internal ID21398884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14806736..14886823hg38UCSC Ensembl
chr16:14900593..14980680hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3880088
hg1980088
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730140
Supporting Variants
SamplesHG00731
Known GenesABCC6P2, NOMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256351
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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