A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609359



Internal ID21557664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26369683..26369683hg38UCSC Ensembl
chr1:26696174..26696174hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064307
SamplesNA19238
Known GenesZNF683
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609359
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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