A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584595



Internal ID16372004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226472641..226481238hg38UCSC Ensembl
Innerchr2:227337357..227345954hg19UCSC Ensembl
Innerchr2:227045601..227054198hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg388598
hg198598
hg188598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7318n54
Supporting Variantsnssv933279
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584595
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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