A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584432



Internal ID16371841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:214043568..214203029hg38UCSC Ensembl
Innerchr2:214908292..215067753hg19UCSC Ensembl
Innerchr2:214616537..214775998hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38159462
hg19159462
hg18159462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv931191
Samples
Known GenesSPAG16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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