A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559138



Internal ID22427941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13649378..13649378hg38UCSC Ensembl
chr10:13691378..13691378hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14332437
SamplesHG00731
Known GenesFRMD4A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559138
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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