A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018755



Internal ID21928098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2583786..2583860hg38UCSC Ensembl
chr7:2623420..2623494hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560259
Samples
Known GenesIQCE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018755
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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