A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570069



Internal ID21518433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181094859..181095052hg38UCSC Ensembl
chr2:181959586..181959779hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110748
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570069
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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