A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609409



Internal ID21557714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81734005..81734005hg38UCSC Ensembl
chr1:82199690..82199690hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067274
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609409
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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