A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583189



Internal ID21531710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35224516..35224591hg38UCSC Ensembl
chr7:35264128..35264203hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158099
SamplesHG00731
Known GenesTBX20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583189
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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