A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360866



Internal ID22586535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77916904..77916904hg38UCSC Ensembl
chr10:79676662..79676662hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959600
Supporting Variants
Samples
Known GenesDLG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360866
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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