A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877085



Internal ID22652048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3122639..3150671hg38UCSC Ensembl
chr16:3172640..3200672hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3828033
hg1928033
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478304
Samples
Known GenesZNF213
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877085
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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