A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752728



Internal ID21392866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50302405..50330404hg38UCSC Ensembl
chr7:50342001..50370000hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3828000
hg1928000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435287
Supporting Variants
SamplesSMI041
Known GenesIKZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752728
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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