A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011366



Internal ID19100583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48171930..48184627hg38UCSC Ensembl
Innerchr4:48173947..48186644hg19UCSC Ensembl
Innerchr4:47868704..47881401hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3812698
hg1912698
hg1812698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5203n100
Supporting Variantsnssv3625136, nssv3625135
Samples
Known GenesTEC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011366
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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