A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375491



Internal ID22264244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35181412..35181412hg38UCSC Ensembl
chr15:35473613..35473613hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560444
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375491
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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