A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305409



Internal ID22274065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15390813..15390907hg38UCSC Ensembl
chr3:15432320..15432414hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203992
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305409
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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