A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584038



Internal ID16371447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:187505505..187585409hg38UCSC Ensembl
Innerchr2:188370232..188450136hg19UCSC Ensembl
Innerchr2:188078477..188158381hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3879905
hg1979905
hg1879905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv928244
Samples
Known GenesTFPI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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