A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389366



Internal ID22447236
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 StatusS
Merged Variantsnsv5929562
Supporting Variants
Samples
Known GenesATF7IP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389366
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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