A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628756



Internal ID21577061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38087571..38087571hg38UCSC Ensembl
chr10:38376499..38376499hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070197
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628756
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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