A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590448



Internal ID16377857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63284124..63286952hg38UCSC Ensembl
Innerchr3:63269800..63272628hg19UCSC Ensembl
Innerchr3:63244840..63247668hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg382829
hg192829
hg182829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963561
Samples
Known GenesSYNPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590448
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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