A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258051



Internal ID21400286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48616678..48617564hg38UCSC Ensembl
chr16:48650589..48651475hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730186
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258051
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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