A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010490



Internal ID21919833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55409158..55409230hg38UCSC Ensembl
chr7:55476851..55476923hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574491
Samples
Known GenesLANCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010490
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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