A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954202



Internal ID16956389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:225018534..225018650hg38UCSC Ensembl
Outerchr2:225883251..225883367hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003853
SamplesBILGI_BIOE
Known GenesDOCK10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954202
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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