A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109429



Internal ID21467783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160573724..160573724hg38UCSC Ensembl
chr2:161430235..161430235hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605362
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109429
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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