A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950019



Internal ID17298893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184751413..184758212hg38UCSC Ensembl
Outerchr3:184469201..184476000hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996566
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950019
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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