A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110560



Internal ID21506221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16895049..16895049hg38UCSC Ensembl
chr2:17076316..17076316hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604849
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110560
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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