A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332571



Internal ID22262629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13867651..13867651hg38UCSC Ensembl
chr10:13909651..13909651hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559244
Supporting Variants
SamplesNA19238
Known GenesFRMD4A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332571
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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