A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525937



Internal ID22395316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109424945..109425036hg38UCSC Ensembl
chr1:109967567..109967658hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14284998, nssv14284999, nssv14285000
SamplesNA19238, NA19239, NA19240
Known GenesPSMA5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525937
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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