A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955337



Internal ID17304210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126500058..126510457hg38UCSC Ensembl
Outerchr3:126218901..126229300hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001454
SamplesBILGI_BIOE
Known GenesUROC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955337
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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