A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584596



Internal ID16372005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226472641..226482648hg38UCSC Ensembl
Innerchr2:227337357..227347364hg19UCSC Ensembl
Innerchr2:227045601..227055608hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3810008
hg1910008
hg1810008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7318n54
Supporting Variantsnssv933280
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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