A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640627



Internal ID21588932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:322878..322878hg38UCSC Ensembl
chr10:368818..368818hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070126, nssv17070127
SamplesHG00732, NA12329
Known GenesDIP2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640627
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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