A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008556



Internal ID19097773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89356604..89371069hg38UCSC Ensembl
Innerchr3:89405754..89420219hg19UCSC Ensembl
Innerchr3:89488444..89502909hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3814466
hg1914466
hg1814466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4808n100
Supporting Variantsnssv3735163, nssv3735162
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)nsv1008556
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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