A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606388



Internal ID21554693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72122730..72122730hg38UCSC Ensembl
chr3:72171881..72171881hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137300
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606388
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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