A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014536



Internal ID19103754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89356604..89370219hg38UCSC Ensembl
Innerchr3:89405754..89419369hg19UCSC Ensembl
Innerchr3:89488444..89502059hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3813616
hg1913616
hg1813616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4808n100
Supporting Variantsnssv3603179, nssv3603197, nssv3603190, nssv3735159, nssv3603188, nssv3603187, nssv3603194, nssv3603192, nssv3603171, nssv3603183, nssv3603184, nssv3735161, nssv3603191, nssv3603178, nssv3735151, nssv3735150, nssv3603195, nssv3735154, nssv3603181, nssv3603177, nssv3735158, nssv3603196, nssv3735160, nssv3603198, nssv3735155, nssv3603189, nssv3603173, nssv3603193, nssv3735148, nssv3735149, nssv3735157, nssv3603174, nssv3735156, nssv3735153, nssv3603176, nssv3735152, nssv3603172, nssv3603185, nssv3603180, nssv3603182, nssv3603175, nssv3603186
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)nsv1014536
Frequency
Sample Size11257
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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