A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046385



Internal ID19135604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28384121..28480307hg38UCSC Ensembl
Innerchr11:28405668..28501854hg19UCSC Ensembl
Innerchr11:28362244..28458430hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3896187
hg1996187
hg1896187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1084n100
Supporting Variantsnssv3512911
Samples
Known GenesMIR8068
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046385
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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