A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572938



Internal ID21521334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101692130..101700283hg38UCSC Ensembl
chr3:101410974..101419127hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg388154
hg198154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129836
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572938
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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