A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730186



Internal ID21400997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48616678..48617568hg38UCSC Ensembl
chr16:48650589..48651479hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258051, nssv16257612, nssv16256355
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730186
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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