A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954882



Internal ID17303755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:71504850..71507649hg38UCSC Ensembl
Outerchr3:71554001..71556800hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001410
SamplesBILGI_BIOE
Known GenesFOXP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954882
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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