A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591432



Internal ID16378841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:124886011..124887249hg38UCSC Ensembl
Innerchr3:124604858..124606096hg19UCSC Ensembl
Innerchr3:126087548..126088786hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg381239
hg191239
hg181239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971811
Samples
Known GenesITGB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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