A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018355



Internal ID21927698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142945649..142945906hg38UCSC Ensembl
chr7:142642736..142642993hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570006
Samples
Known GenesKEL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018355
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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