A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640464



Internal ID21588769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76191190..76191190hg38UCSC Ensembl
chr5:75487015..75487015hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg382666
hg192666
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146783
SamplesHG00732
Known GenesSV2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640464
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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