A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590700



Internal ID16378109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75422703..75481744hg38UCSC Ensembl
Innerchr3:75471854..75530895hg19UCSC Ensembl
Innerchr3:75554544..75613585hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3859042
hg1959042
hg1859042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965775
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590700
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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