A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203992



Internal ID22352914
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305409, nssv14305410, nssv14305408
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203992
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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