A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896482



Internal ID22671576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57107372..57109570hg38UCSC Ensembl
chr4:57973538..57975736hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382199
hg192199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425043
Samples
Known GenesIGFBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896482
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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