A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564268



Internal ID21888623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67340123..67420427hg38UCSC Ensembl
chr7:66805110..66885414hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3880305
hg1980305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564268
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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