A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565189



Internal ID21889544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83399349..83399349hg38UCSC Ensembl
chr7:83028665..83028665hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079763
Supporting Variants
Samples
Known GenesSEMA3E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565189
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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