A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955311



Internal ID16957498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:2512217..2518716hg38UCSC Ensembl
Outerchr3:2553901..2560400hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001331
SamplesBILGI_BIOE
Known GenesCNTN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955311
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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