A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887152



Internal ID22662144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15601629..15603287hg38UCSC Ensembl
chr16:15695486..15697144hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg381659
hg191659
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476339
Samples
Known GenesKIAA0430
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887152
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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