A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596091



Internal ID18894372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75379820..75497567hg38UCSC Ensembl
Innerchr3:75428971..75546718hg19UCSC Ensembl
Innerchr3:75511661..75629408hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38117748
hg19117748
hg18117748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004717
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596091
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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