A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639830



Internal ID21588135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14568337..14568337hg38UCSC Ensembl
chr10:14610336..14610336hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069187
SamplesHG00731
Known GenesFAM107B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639830
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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