A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583154



Internal ID16023877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:132451024..132495813hg38UCSC Ensembl
Innerchr2:133208597..133253386hg19UCSC Ensembl
Innerchr2:132925067..132969856hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3844790
hg1944790
hg1844790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151302
SamplesHGDP00998
Known GenesGPR39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583154
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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