A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579604



Internal ID21528085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102304627..102304747hg38UCSC Ensembl
chr4:103225784..103225904hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121681
SamplesHG02818
Known GenesSLC39A8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579604
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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