A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376760



Internal ID22164545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27363484..27363609hg38UCSC Ensembl
chr15:27608630..27608755hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216188
Supporting Variants
SamplesHG00514
Known GenesGABRG3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376760
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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