A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590651



Internal ID16378060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75370585..75574858hg38UCSC Ensembl
Innerchr3:75419736..75624009hg19UCSC Ensembl
Innerchr3:75502426..75706699hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38204274
hg19204274
hg18204274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8383n54
Supporting Variantsnssv965640
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590651
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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