A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096247



Internal ID21492503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45262516..45262516hg38UCSC Ensembl
chr17:43339883..43339883hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659109
Supporting Variants
SamplesNA19238
Known GenesMAP3K14-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096247
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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