A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568459



Internal ID21760502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5493930..5494042hg38UCSC Ensembl
chr7:5533561..5533673hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011998
Supporting Variants
Samples
Known GenesFBXL18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568459
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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