A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590458



Internal ID16031181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63529804..63530210hg38UCSC Ensembl
Innerchr3:63515480..63515886hg19UCSC Ensembl
Innerchr3:63490520..63490926hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38407
hg19407
hg18407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963572
Samples
Known GenesSYNPR, SYNPR-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590458
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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