A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733698



Internal ID19031979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75400451..75451601hg38UCSC Ensembl
Innerchr3:75449602..75500752hg19UCSC Ensembl
Innerchr3:75532292..75583442hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3851151
hg1951151
hg1851151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999439
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)nssv3733698
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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