A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609551



Internal ID21557856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37102938..37102938hg38UCSC Ensembl
chr1:37568539..37568539hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065182
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609551
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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