A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047138



Internal ID18789669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95660745..95677310hg38UCSC Ensembl
Innerchr14:96127082..96143647hg19UCSC Ensembl
Innerchr14:95196835..95213400hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3816566
hg1916566
hg1816566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532625
Samples
Known GenesTCL6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047138
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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