A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559509



Internal ID332541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30417625..30419422hg38UCSC Ensembl
chr16:30428946..30430743hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381798
hg191798
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707680
Samples
Known GenesZNF771
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559509
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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