A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574530



Internal ID21522946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182004476..182004558hg38UCSC Ensembl
chr3:181722264..181722346hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129424
SamplesNA19650
Known GenesLOC100996490
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574530
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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