A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590663



Internal ID16378072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75388738..75481744hg38UCSC Ensembl
Innerchr3:75437889..75530895hg19UCSC Ensembl
Innerchr3:75520579..75613585hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3893007
hg1993007
hg1893007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8381n54
Supporting Variantsnssv965671, nssv965670, nssv965672
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590663
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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