A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088737



Internal ID21464760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1076268..1076268hg38UCSC Ensembl
chr16:1126268..1126268hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664346
Supporting Variants
SamplesHG03065
Known GenesSSTR5, SSTR5-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088737
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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