A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119892



Internal ID21449643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149023924..149023924hg38UCSC Ensembl
chr3:148741711..148741711hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611240
Supporting Variants
SamplesHG01114
Known GenesGYG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119892
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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