A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584306



Internal ID16371715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208890335..209001671hg38UCSC Ensembl
Innerchr2:209755059..209866395hg19UCSC Ensembl
Innerchr2:209463304..209574640hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38111337
hg19111337
hg18111337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151165
SamplesNINDS_103
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584306
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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