A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134914



Internal ID21449814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1581227..1581227hg38UCSC Ensembl
chr4:1582954..1582954hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617833
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134914
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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