A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735167



Internal ID19033448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89356604..89371326hg38UCSC Ensembl
Innerchr3:89405754..89420476hg19UCSC Ensembl
Innerchr3:89488444..89503166hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3814723
hg1914723
hg1814723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008481
Supporting Variants
Samples
Known GenesEPHA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3735167
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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