A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576202



Internal ID21524638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13664776..13668893hg38UCSC Ensembl
chr3:13706276..13710393hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384118
hg194118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137712
SamplesHG03486
Known GenesLINC00620
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576202
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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