A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576172



Internal ID21524607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2905248..2905307hg38UCSC Ensembl
chr2:2909020..2909079hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112891
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576172
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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