A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525177



Internal ID22394553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225035588..225035649hg38UCSC Ensembl
chr2:225900305..225900366hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5016n152
Supporting Variantsnssv14297505, nssv14297506
SamplesNA19239, NA19240
Known GenesDOCK10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525177
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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