A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015183



Internal ID21924526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83017563..83020601hg38UCSC Ensembl
chr7:82646879..82649917hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575757
Samples
Known GenesPCLO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015183
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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