A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435288



Internal ID21397290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50343303..50369302hg38UCSC Ensembl
chr7:50411001..50437000hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3826000
hg1926000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754497
SamplesSMI041
Known GenesIKZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435288
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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