A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124109



Internal ID21418710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124737853..124737853hg38UCSC Ensembl
chr4:125659008..125659008hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616300
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124109
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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