A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955589



Internal ID17304462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:49480472..49480964hg38UCSC Ensembl
Outerchr3:49517905..49518397hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004591
SamplesBILGI_BIOE
Known GenesDAG1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955589
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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