A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634813



Internal ID21583118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77586986..77586986hg38UCSC Ensembl
chr5:76882811..76882811hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158226
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634813
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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