A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584027



Internal ID16371436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185986497..186089700hg38UCSC Ensembl
Innerchr2:186851224..186954427hg19UCSC Ensembl
Innerchr2:186559469..186662672hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38103204
hg19103204
hg18103204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7228n54
Supporting Variantsnssv928235
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584027
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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