A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440996



Internal ID22498866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107476183..107476183hg38UCSC Ensembl
chr7:107116628..107116628hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963689
Supporting Variants
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440996
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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