A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580176



Internal ID21528664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100203835..100206090hg38UCSC Ensembl
chr3:99922679..99924934hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg382256
hg192256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138525
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580176
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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