A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576651



Internal ID21768694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35838282..35838334hg38UCSC Ensembl
chr7:35877892..35877944hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016636
Supporting Variants
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576651
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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