A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351204



Internal ID22576873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109960747..109960747hg38UCSC Ensembl
chr10:111720505..111720505hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952900
Supporting Variants
Samples
Known GenesADD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351204
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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