A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629562



Internal ID21577867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38170158..38170158hg38UCSC Ensembl
chr10:38459086..38459086hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070206
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629562
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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