A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754497



Internal ID21392635
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 StatusS
Merged Variantsnsv4435288
Supporting Variants
SamplesSMI041
Known GenesIKZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754497
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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