A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929562



Internal ID22704818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10448867..10451020hg38UCSC Ensembl
chr16:10542724..10544877hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389366
Samples
Known GenesATF7IP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929562
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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