A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590665



Internal ID16378074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75388738..75537504hg38UCSC Ensembl
Innerchr3:75437889..75586655hg19UCSC Ensembl
Innerchr3:75520579..75669345hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38148767
hg19148767
hg18148767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8382n54
Supporting Variantsnssv965676
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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