A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632203



Internal ID21580508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52866318..52866318hg38UCSC Ensembl
chr5:52162152..52162152hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128187
SamplesNA19238
Known GenesITGA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632203
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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