A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119657



Internal ID21506796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21980910..21980910hg38UCSC Ensembl
chr4:21982533..21982533hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623162
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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