A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14378557



Internal ID22169541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90993100..90993227hg38UCSC Ensembl
chr15:91536330..91536457hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224310
Supporting Variants
SamplesHG00514
Known GenesPRC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14378557
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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