A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484134



Internal ID261554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87898777..87898860hg38UCSC Ensembl
chr7:87528092..87528175hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002033
Samples
Known GenesDBF4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484134
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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