A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391497



Internal ID21382527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10452924..10453176hg38UCSC Ensembl
chr16:10546781..10547033hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705999
Samples
Known GenesATF7IP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391497
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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